GB1256416A - RECOVERY OF alpha-AMINO-epsilon-CAPROLACTAM MONOHYDROCHLORIDE OF ENHANCED OPTICAL PURITY - Google Patents
RECOVERY OF alpha-AMINO-epsilon-CAPROLACTAM MONOHYDROCHLORIDE OF ENHANCED OPTICAL PURITYInfo
- Publication number
- GB1256416A GB1256416A GB2382769A GB2382769A GB1256416A GB 1256416 A GB1256416 A GB 1256416A GB 2382769 A GB2382769 A GB 2382769A GB 2382769 A GB2382769 A GB 2382769A GB 1256416 A GB1256416 A GB 1256416A
- Authority
- GB
- United Kingdom
- Prior art keywords
- monohydrochloride
- caprolactam
- recovery
- amino
- salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/02—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D223/06—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D223/12—Nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
1,256,416. Aminocaprolactam hydrochloride; lysine. STAMICARBON N.V. 9 May, 1969 [14 May, 1968], No. 23827/69. Heading C2C. α - Amino - # - caprolactam monohydrochloride of enhanced optical purity is obtained from the relatively optically impure salt by (1) subjecting the relatively impure monohydrochloride to fractional crystallization arid recovering the pure salt as crystals or (2) subjecting the impure monohydrochloride to extraction with a solvent whereby the pure salt remains as a solid after extraction. Specified solvents for both processes are water and aqueous ethanol and methanol. Crystallization and extraction are conducted at 15-65‹ C. when water is used. Examples describe the recovery of the pure L- and D-salts. The L-salt may be hydrolysed to L-lysine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL6806784A NL6806784A (en) | 1968-05-14 | 1968-05-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1256416A true GB1256416A (en) | 1971-12-08 |
Family
ID=19803621
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2382769A Expired GB1256416A (en) | 1968-05-14 | 1969-05-09 | RECOVERY OF alpha-AMINO-epsilon-CAPROLACTAM MONOHYDROCHLORIDE OF ENHANCED OPTICAL PURITY |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE732730A (en) |
FR (1) | FR2008511A1 (en) |
GB (1) | GB1256416A (en) |
NL (1) | NL6806784A (en) |
-
1968
- 1968-05-14 NL NL6806784A patent/NL6806784A/xx unknown
-
1969
- 1969-05-08 BE BE732730D patent/BE732730A/xx unknown
- 1969-05-09 GB GB2382769A patent/GB1256416A/en not_active Expired
- 1969-05-14 FR FR6915695A patent/FR2008511A1/fr not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
FR2008511A1 (en) | 1970-01-23 |
NL6806784A (en) | 1969-11-18 |
BE732730A (en) | 1969-11-10 |
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