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Sodium Hydroxide → 3-(2-o-Tolylamino-benzoxazol-6-yl)propanoic acid

HRID 987528
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인쇄 미리보기

반응식

HRID 987528 반응식
[C:1]1([CH3:24])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH:7][C:8]1[O:9][C:10]2[CH:16]=[C:15]([CH2:17][CH2:18][C:19]([O:21]CC)=[O:20])[CH:14]=[CH:13][C:11]=2[N:12]=1.[OH-].[Na+]>CO>[C:1]1([CH3:24])[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[NH:7][C:8]1[O:9][C:10]2[CH:16]=[C:15]([CH2:17][CH2:18][C:19]([OH:21])=[O:20])[CH:14]=[CH:13][C:11]=2[N:12]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 18008945Ethyl 3-(2-o-tolylamino-benzoxazol-6-yl)propanoate

생성물 1

HCID 180089523-(2-o-Tolylamino-benzoxazol-6-yl)propanoic acid

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
40 °C

실험 절차

A solution of ethyl 3-(2-o-tolylamino-benzoxazol-6-yl)propanoate (Reference Example 15) in methanol (50 ml) was treated with aqueous sodium hydroxide (5 ml, 1M). After stirring at 40° C. for 2 hours the mixture was evaporated to low volume and partitioned between ethyl acetate (50 ml) and water (50 ml). The aqueous phase was separated and acidified with aqueous hydrochloric acid (10 ml, 1M). The resulting precipitate was dried at 60° C. to give the title compound (1.1 g).

후처리

  1. customwas evaporated to low volume
  2. custompartitioned between ethyl acetate (50 ml) and water (50 ml)
  3. customThe aqueous phase was separated
  4. customThe resulting precipitate was dried at 60° C.

출처 및 근거

ORD 기록
ord-b38d8f145dad4f319171d8ce9861c74b
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06632814B1

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