IP Library Granted Patent US 10,870,632
Granted Patent B2
US 10,870,632 · App. 14/276,165 · Granted Dec 22, 2020

Process for producing an extract containing tetrahydrocannabinol and cannabidiol from cannabis plant material, and cannabis extracts

Inventor: Adam Mueller (Coburg, DE)
C07D311/80A61K31/35A61K36/185Y02P20/54
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,870,632
App. No.
14/276,165
Granted
Dec 22, 2020
Kind
B2
Abstract

The invention relates to a method for producing an extract from cannabis plant matter, containing tetrahydrocannabinol, cannabidiol and optionally the carboxylic acids thereof. According to said method, the dried pint matter is ground and subjected to a CO 2 extraction and the primary extract obtained is separated. The invention method permits Δ 8 or Δ 9 tetrahydrocannabinol to be selectively obtained both from industrial hemp and from drug-producing hemp, optionally after dissolving the primary extract in ethanol, separating undesirable waxes and removing the solvent under reduced pressure.

Claims (30)

1. A process for producing an extract containing Tetrahydrocannabinol (THC) and/or cannabidiol (CBD), and optionally the carboxylic acids thereof, from a cannabis plant material or a primary extract thereof, said process comprising:

(1) subjecting the cannabis plant material or primary extract thereof to CO 2 in liquefied form under subcritical pressure and temperature conditions to extract cannabinoid components; and

(2) reducing the pressure and/or temperature to separate tetrahydrocannabinol and/or cannabidiol, and optionally the carboxylic acids thereof, from the CO 2 .

2. The process according to claim 1 , further comprising subjecting the CO 2 extracted from step (2) to increased pressure and temperature and recycling said CO 2 to step (1).

3. The process according to claim 1 , wherein in step (1) the CO 2 in liquefied form is at a pressure of 70 bar or less.

4. The process according to claim 3 , wherein in step (1) the CO 2 in liquefied form is at a temperature of between about 20° C. to about 30° C.

5. The process according to claim 1 , wherein in step (1) the CO 2 in liquefied form is at a pressure of about 60 bar.

6. The process according to claim 1 , wherein in step (2) the CO 2 in liquefied form is at a pressure of about 55 bar or less.

7. The process according to claim 3 , wherein in step (2) the CO 2 in liquefied form is at a pressure of about 55 bar or less and a temperature of about 20° C. or less.

8. The process according to claim 1 , which further comprises separating monoterpenes and sequiterpenes from the tetrahydrocannabinol and cannabidiol using a separator.

9. The process according to claim 1 , wherein the cannabis plant material contains 0.5% or less of Δ 9 -THC based on the dry plant mass.

10. The process according to claim 1 , wherein an adsorbent for extracting components other than tetrahydrocannabinol, cannabidiol and optionally the carboxylic acids thereof is arranged downstream in terms of the CO 2 flow.

11. The process according to claim 10 , wherein the adsorbent is selected from the group consisting of silica gel, diatomaceous earth, bentonites, bleaching earth, activated carbons, magnesium oxide and alumina, as well as mixtures thereof.

12. The process according to claim 11 , wherein the absorbent is for extracting components selected from the group consisting of alkaloids, flavonoids, monoterpenes, sesquiterpenes, and chlorophylls.

13. The process according to claim 1 , further comprising a step of decarboxylating cannabinoid carboxylic acids in the cannabis plant material or primary extract thereof.

14. A process for producing an extract containing Tetrahydrocannabinol (THC) and/or cannabidiol (CBD) from a cannabis plant material or a primary extract thereof, said process comprising:

(1) decarboxylating cannabinoid carboxylic acids in the cannabis plant material or primary extract thereof;

(2) subjecting the decarboxylated cannabis plant material or primary extract thereof to CO 2 in liquefied form under subcritical pressure and temperature conditions to extract cannabinoid components; and

(3) reducing the pressure and/or temperature to separate tetrahydrocannabinol and/or cannabidiol from the CO 2 .

15. The process according to claim 14 , further comprising subjecting the CO 2 extracted from step (3) to increased pressure and temperature and recycling said CO 2 to step (2).

16. The process according to claim 14 , wherein in step (2) the CO 2 in liquefied form is at a pressure of 70 bar or less.

17. The process according to claim 16 , wherein in step (2) the CO 2 in liquefied form is at a temperature of between about 20° C. to about 30° C.

18. The process according to claim 14 , wherein in step (2) the CO 2 in liquefied form is at a pressure of about 60 bar.

19. The process according to claim 14 , wherein in step (3) the CO 2 in liquefied form is at a pressure of about 55 bar or less.

20. The process according to claim 16 , wherein in step (3) the CO 2 in liquefied form is at a pressure of about 55 bar or less and a temperature of about 20° C. or less.

21. The process according to claim 14 , which further comprises separating monoterpenes and sequiterpenes from the tetrahydrocannabinol and cannabidiol using a separator.

22. The process according to claim 14 , wherein the cannabis plant material contains 0.5% or less of Δ 9 -THC based on the dry plant mass.

23. The process according to claim 14 , wherein an adsorbent for extracting components other than tetrahydrocannabinol, cannabidiol and optionally the carboxylic acids thereof is arranged downstream in terms of the CO 2 flow.

24. The process according to claim 23 , wherein the adsorbent is selected from the group consisting of silica gel, diatomaceous earth, bentonites, bleaching earth, activated carbons, magnesium oxide and alumina, as well as mixtures thereof.

25. The process according to claim 24 , wherein the absorbent is for extracting components selected from the group consisting of alkaloids, flavonoids, monoterpenes, sesquiterpenes, and chlorophylls.

Assignments (7)
RELEASE OF SECURITY INTEREST IN PATENT INTELLECTUAL PROPERTY Recorded Jan 9, 2026
From: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
To: CANOPY GROWTH CORPORATION
Reel/Frame 074281/0925 →
NOTICE OF GRANT OF SECURITY INTEREST Recorded Aug 15, 2024
From: CANOPY GROWTH CORPORATION
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 068654/0264 →
NOTICE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Mar 22, 2021
From: CANOPY GROWTH CORPORATION
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 055683/0826 →
CHANGE OF NAME Recorded Dec 4, 2020
From: BIONORICA ETHICS GMBH
To: SPECTRUM THERAPEUTICS GMBH
Reel/Frame 054600/0136 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2020
From: SPECTRUM THERAPEUTICS GMBH
To: CANOPY GROWTH CORPORATION
Reel/Frame 054547/0815 →
CHANGE OF NAME Recorded Apr 9, 2015
From: DELTA-9-PHARMA GMBH
To: BIONORICA ETHICS GMBH
Reel/Frame 035392/0248 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 3, 2015
From: MUELLER, ADAM
To: DELTA-9-PHARMA GMBH
Reel/Frame 035326/0908 →
Priority Claims (1)
DE 100 51 427 · Oct 17, 2000 · national
Continuity (2)
Continuation 10399362
Related Publication 20140248379A1 · Sep 4, 2014