Ammonia → 2-Amino-3,3-dimethylbutanoic acid

HRID 76843

반응식

HRID 76843 반응식
[OH-].[Na+].[NH2:3][C@@H:4]([C:9]([OH:11])=[O:10])[C:5]([CH3:8])([CH3:7])[CH3:6].[OH-].[NH4+].N>>[NH2:3][CH:4]([C:9]([OH:11])=[O:10])[C:5]([CH3:8])([CH3:7])[CH3:6]

참가 물질

5

실험 절차

A process was developed to racemize D-tert-leucine so that it can be recycled. Use of acids, although caused racemization, resulted in salt formation. It was tedious to obtain free amino acid from such salts. The same drawback was observed when a strong base such as sodium hydroxide was used. However, treating D-tert-leucine with ammonium hydroxide resulted in complete racemization. The reaction has to be conducted at about 80° C. for about 12 hours in an autoclave to prevent the escape of ammonia. The solvent is removed at 55° C. (±5) under reduced pressure to obtain DL-tert-leucine. After the reaction, although ammonium salt of DL-tent-leucine is obtained, during the removal of the solvent, ammonia also is eliminated and free amino acid is obtained.

후처리

  1. customresulted in complete racemization
  2. customThe solvent is removed at 55° C. (±5) under reduced pressure

출처 및 근거

ORD 기록
ord-c4857fc2c7fa4557abce9b560a7bf2c7
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08835676B2

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