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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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ethyl 1-(2-tert-butoxy-2-oxoethyl)-1H-pyrazole-4-carboxylate → [4-(ethoxycarbonyl)-1H-pyrazol-1-yl]acetic acid

HRID 1257420
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HRID 1257420 반응식
C([O:5][C:6](=[O:18])[CH2:7][N:8]1[CH:12]=[C:11]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:10]=[N:9]1)(C)(C)C>FC(F)(F)C(O)=O>[CH2:16]([O:15][C:13]([C:11]1[CH:10]=[N:9][N:8]([CH2:7][C:6]([OH:18])=[O:5])[CH:12]=1)=[O:14])[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 59557976ethyl 1-(2-tert-butoxy-2-oxoethyl)-1H-pyrazole-4-carboxylate

생성물 1

HCID 59557975[4-(ethoxycarbonyl)-1H-pyrazol-1-yl]acetic acid수율 110%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

The compound (17.5 g) obtained in Example 115a was added to trifluoroacetic acid (280 mL), and the mixture was stirred at room temperature for 30 min. The reaction mixture was concentrated under reduced pressure, and the residue was washed with hexane, and dried to give the title compound (15.0 g) as a colorless solid.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. washthe residue was washed with hexane
  3. customdried

출처 및 근거

ORD 기록
ord-09e4e0fb3f704497bab09c9b872ea197
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08461348B2

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