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Trifluoroacetic acid → 2-[5-(Ethoxycarbonyl)-2-oxo-1-azepanyl]butanoic acid

HRID 1452515
노트
인쇄 미리보기

반응식

HRID 1452515 반응식
C([O:5][C:6]([CH:8]([N:11]1[C:17](=[O:18])[CH2:16][CH2:15][CH:14]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:13][CH2:12]1)[CH2:9][CH3:10])=[O:7])(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[CH2:22]([O:21][C:19]([CH:14]1[CH2:13][CH2:12][N:11]([CH:8]([CH2:9][CH3:10])[C:6]([OH:7])=[O:5])[C:17](=[O:18])[CH2:16][CH2:15]1)=[O:20])[CH3:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 23545594Ethyl 1-[1-(tert-butoxycarbonyl)propyl]-7-oxo-4-azepanecarboxylate

생성물 1

HCID 219903032-[5-(Ethoxycarbonyl)-2-oxo-1-azepanyl]butanoic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

In a 25 ml three necked flask fitted with magnetic stirrer and dropping funnel under inert atmosphere, 1 g (3.1 mmoles) of pure ethyl 1-[1-(tert-butoxycarbonyl)propyl]-7-oxo-4-azepanecarboxylate 29 was dissolved in 5 ml of CH2Cl2. The mixture was cooled down to 0° C., 5 ml of trifluoroacetic acid was added. The mixture was kept at 0° C. under stirring for 24 hours, concentrated to dryness and used as such in the next step.

후처리

  1. customwas kept at 0° C.
  2. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-f56fc1cd774142bb9bc1fefd8959685f
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07473697B2

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