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Sodium Hydroxide → 1-((tert-butoxy)carbonyl)-2,3-dihydro-1H-indole-3-carboxylic acid

HRID 863315
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인쇄 미리보기

반응식

HRID 863315 반응식
[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]([C:17]([O:19]CC)=[O:18])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>CO.O>[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]([C:17]([OH:19])=[O:18])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 196977841-tert-Butyl 3-ethyl indoline-1,3-dicarboxylate

생성물 1

HCID 196977501-((tert-butoxy)carbonyl)-2,3-dihydro-1H-indole-3-carboxylic acid

시약·촉매·용매 1

HCID 22242641Methanol--water (1/1)용매

반응 조건

온도
50 °C

실험 절차

A mixture of 0.7 g of ethyl 1-(tert-butoxycarbonyl)indoline-3(R,S)-carboxylate (Example 97d) in 18 ml of methanol/water (1:1) and 2.9 ml of a 1N sodium hydroxide solution is stirred at 50° C. for 3 h. After the methanol has been removed in vacuo, the aqueous phase is brought to pH 2 and extracted with ethyl acetate. Customary further working up gives the title compound as a white solid: Rf (hexane/ethyl acetate/glacial acetic acid (75:25:1))=0.23.

후처리

  1. customAfter the methanol has been removed in vacuo
  2. extractionextracted with ethyl acetate

출처 및 근거

ORD 기록
ord-9c4213d9f7e2473fb550065d7916dcb8
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05719141

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