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Trifluoroacetic acid → [1-(2-Ethoxy-2-oxoethyl)-3-nitro-1H-indol-4-yl]acetic Acid

HRID 641406
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반응식

HRID 641406 반응식
[CH2:1]([O:3][C:4](=[O:26])[CH2:5][N:6]1[C:14]2[C:9](=[C:10]([CH2:15][C:16]([O:18]C(C)(C)C)=[O:17])[CH:11]=[CH:12][CH:13]=2)[C:8]([N+:23]([O-:25])=[O:24])=[CH:7]1)[CH3:2].C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH2:1]([O:3][C:4](=[O:26])[CH2:5][N:6]1[C:14]2[C:9](=[C:10]([CH2:15][C:16]([OH:18])=[O:17])[CH:11]=[CH:12][CH:13]=2)[C:8]([N+:23]([O-:25])=[O:24])=[CH:7]1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 57426201tert-Butyl[1-(2-ethoxy-2-oxoethyl)-3-nitro-1H-indol-4-yl]acetate

생성물 1

HCID 57426202[1-(2-Ethoxy-2-oxoethyl)-3-nitro-1H-indol-4-yl]acetic Acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of tert-butyl [1-(2-ethoxy-2-oxoethyl)-3-nitro-1H-indol-4-yl]acetate from Step E (300 mg, 0.828 mmol) in CH2Cl2 (1 mL) was added TFA (0.63 mL, 8.28 mmol). The mixture was stirred at ambient temperature for 1 h then concentrated in vacuo to give the title compound. MS: m/z=307 (M+1).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. concentrationthen concentrated in vacuo

출처 및 근거

ORD 기록
ord-cc2f41b788da49cebac35d8ad886390e
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07696192B2

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