IP Library Granted Patent US 9,718,798
Granted Patent B2
US 9,718,798 · App. 14/852,152 · Granted Aug 1, 2017

Solid forms of 5-(halomethyl)furfural and methods for preparing thereof

Inventors: Shawn M. Browning (Sacramento, CA); Makoto N. Masuno (Elk Grove, CA); John Bissell, II (Sacramento, CA); Benjamin F. Nicholson (Sacramento, CA)
Assignee: MICROMIDAS, INC.
C07D307/46C07D307/18C07D307/48
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Quick Facts
Patent No.
US 9,718,798
App. No.
14/852,152
Granted
Aug 1, 2017
Kind
B2
Abstract

Provided are solid forms of 5-(halomethyl)furfural, including a crystalline form of 5-(chloromethyl)furfural. Provided are also methods for preparing solid forms of 5-(halomethyl)furfural by crystallization using certain solvents.

Claims (27)

1. A composition comprising:

a crystalline form of 5-(chloromethyl)furfural, wherein the crystalline form is Form I having an X-ray diffraction (XRD) pattern comprising at least peaks at about 16.6 degrees 2θ and about 27.0 degrees 2θ; and

one or more alkyl phenyl solvents.

2. The composition of claim 1 , wherein one or more of the alkyl phenyl solvents are linear alkylbenzenes.

3. The composition of claim 1 , wherein one or more of the alkyl phenyl solvents are selected from the group consisting of dodecylbenzene, pentylbenzene, and hexylbenzene, or any combinations or mixtures thereof.

4. The composition of claim 1 , wherein the XRD pattern of Form I further comprises at least one additional peak at about 20.7 degrees 2θ, about 22.0 degrees 2θ, about 30.3 degrees 2θ, or about 31.1 degrees 2θ.

5. The composition of claim 1 , wherein Form I is a monoclinic crystal system.

6. The composition of claim 1 , wherein less than 20% of the composition is amorphous 5-(chloromethyl)furfural.

7. The composition of claim 1 , wherein less than 10% of the composition is amorphous 5-(chloromethyl)furfural.

8. The composition of claim 1 , wherein less than 1% of the composition is amorphous 5-(chloromethyl)furfural.

9. The composition of claim 1 , wherein one or more of the alkyl phenyl solvents have one alkyl chain attached to one benzene ring.

10. The composition of claim 1 , wherein one or more of the alkyl phenyl solvents have two or more alkyl chains attached to one benzene ring.

11. The composition of claim 1 , wherein one or more of the alkyl phenyl solvents comprise an alkyl-substituted fused benzene ring system.

12. The composition of claim 1 , wherein one or more of the alkyl phenyl solvents have two or more phenyl rings attached to one alkyl chain.

13. A composition comprising:

a crystalline form of 5-(chloromethyl)furfural, wherein the crystalline form is Form I having an X-ray diffraction (XRD) pattern substantially as shown in FIG. 1 ; and

one or more alkyl phenyl solvents.

14. The composition of claim 13 , wherein Form I is a monoclinic crystal system.

15. The composition of claim 13 , wherein less than 20% of the composition is amorphous 5-(chloromethyl)furfural.

16. The composition of claim 13 , wherein less than 10% of the composition is amorphous 5-(chloromethyl)furfural.

17. The composition of claim 13 , wherein less than 1% of the composition is amorphous 5-(chloromethyl)furfural.

18. The composition of claim 13 , wherein one or more of the alkyl phenyl solvents are linear alkylbenzenes.

19. The composition of claim 13 , wherein one or more of the alkyl phenyl solvents are selected from the group consisting of dodecylbenzene, pentylbenzene, and hexylbenzene, or any combinations or mixtures thereof.

20. The composition of claim 13 , wherein one or more of the alkyl phenyl solvents have one alkyl chain attached to one benzene ring.

21. The composition of claim 13 , wherein one or more of the alkyl phenyl solvents have two or more alkyl chains attached to one benzene ring.

22. The composition of claim 13 , wherein one or more of the alkyl phenyl solvents comprise an alkyl-substituted fused benzene ring system.

23. The composition of claim 13 , wherein one or more of the alkyl phenyl solvents have two or more phenyl rings attached to one alkyl chain.

Assignments (3)
CHANGE OF NAME Recorded Feb 14, 2022
From: MICROMIDAS, INC.
To: ORIGIN MATERIALS OPERATING, INC.
Reel/Frame 059109/0403 →
SECURITY INTEREST Recorded Nov 12, 2019
From: MICROMIDAS, INC,
To: PM OPERATING, LTD.
Reel/Frame 050980/0661 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2017
From: BROWNING, SHAWN M.; MASUNO, MAKOTO N.; BISSELL, JOHN, II; NICHOLSON, BENJAMIN F.
To: MICROMIDAS, INC.
Reel/Frame 042800/0466 →
Continuity (3)
Continuation PCTUS2014024940 · Mar 12, 2014
Provisional Application 61785749 · Mar 14, 2013
Related Publication 20160002190A1 · Jan 7, 2016