IP Library › Granted Patent US 10,081,651
Granted Patent B2
US 10,081,651 · App. 15/502,372 · Granted Sep 25, 2018

Chlorination of sucrose-6-esters

Inventors: Thomas Eilers (Arlington Heights, IL); Halil Aktas (NB Zaandam, NL)
Assignee: Tate & Lyle Technology Limited
C07H5/02C07H13/04
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Quick Facts
Patent No.
US 10,081,651
App. No.
15/502,372
Granted
Sep 25, 2018
Kind
B2
Abstract

There is provided a method for the chlorination of a sucrose-6-acylate to produce a 4,1′,6′-trichloro-4,1′,6′-trideoxy-galactosucrose-6-acylate, wherein said method comprises the following steps (i) to (v): (i) providing a first component comprising sucrose-6-acylate; (ii) providing a second component comprising a chlorinating agent; (iii) combining said first component and said second component to afford a mixture; (iv) heating said mixture for a heating period in order to provide chlorination of sucrose-6-acylate at the 4, 1′ and 6′ positions thereof; (v) quenching said mixture to produce a 4,1′,6′-trichloro-4,1′,6′-trideoxy-galactosucrose-6-acylate; wherein at least one of said first component and said second component comprises a reaction vehicle, and said reaction vehicle comprises a tertiary amide; and wherein said mixture comprises a cosolvent during a least a portion of the heating period of step (iv), wherein said cosolvent comprises dimethylacetamide (DMAc).

Claims (20)

1. A method for the chlorination of a sucrose-6-acylate to produce a 4,1′,6′-trichloro-4,1′,6′-trideoxy-galactosucrose-6-acylate, wherein said method comprises the following steps (i) to (v):

(i) providing a first component comprising sucrose-6-acylate;

(ii) providing a second component comprising a chlorinating agent;

(iii) combining said first component and said second component to afford a mixture;

(iv) heating said mixture for a heating period in order to provide chlorination of sucrose-6-acylate at the 4, 1′ and 6′ positions thereof;

(v) quenching said mixture to produce a 4,1′,6′-trichloro-4,1′,6′-trideoxy-galactosucrose-6-acylate;

wherein at least one of said first component and said second component comprises dimethylformamide (DMF); and

wherein dimethylacetamide (DMAc) is added to said mixture either (a) after step (iii) and before step (iv) or (b) during step (iv).

2. The method according to claim 1 , wherein both of said first component and said second component comprise dimethylformamide (DMF).

3. The method according to claim 1 , wherein said mixture additionally comprises sulfolane and/or perfluorooctane during at least a portion of the heating period of step (iv).

4. The method according to claim 1 , wherein at least one of DMAc, sulfolane, perfluorooctane, or a mixture thereof is added to the mixture after step (iii) and before step (iv).

5. The method according to claim 1 , wherein at least one of DMAc, sulfolane, perfluorooctane, or a mixture thereof is added to the mixture during step (iv).

6. The method according to claim 5 , wherein the at least one of DMAc, sulfolane, perfluorooctane, or a mixture thereof is added once the mixture temperature Is greater than or equal to about 55° C.

7. The method according to claim 3 , wherein;

the DMAc is added to the mixture after step (iii) and before step (iv) and/or during step (iv); and

the perfluorooctane and/or sulfolane is present in the first and/or second components, and/or is added during step (iii).

8. The method according to claim 7 wherein the DMAc is added to the mixture during step (iv) once the mixture temperature is greater than or equal to about 55° C.

9. The method according to claim 1 , wherein one of DMAc, or DMAc and perfluorooctane, or DMAC and sulfolane or DMAc, perfluorooctane and sulfolane is present in the mixture during at least a portion of the heating period of step (iv).

10. The method according to claim 1 , which further comprises a step (vi) of converting at least a portion of said 4,1′,6′-trichloro-4,1′,6′-trideoxy-galactosucrose-6-acylate to sucralose.

11. The method according to claim 10 , which further comprises a step (vii) of isolating and purifying the sucralose.

Assignments (2)
REGISTER CHANGE OF ADDRESS Recorded May 27, 2022
From: TATE & LYLE TECHNOLOGY LIMITED
To: TATE & LYLE TECHNOLOGY LIMITED
Reel/Frame 060203/0469 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2017
From: EILERS, THOMAS; AKTAS, HALIL
To: TATE & LYLE TECHNOLOGY LIMITED
Reel/Frame 042303/0057 →
Continuity (2)
Provisional Application 62035066 · Aug 8, 2014
Related Publication 20170233424A1 · Aug 17, 2017