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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Butanoic acid, 3-oxo-4-(phenylmethoxy)-, 1,1-dimethylethyl ester → HCID 13422882, 화합물

HRID 2290418
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HRID 2290418 반응식
C([O:8][CH2:9][C:10](=[O:19])[CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])C1C=CC=CC=1>CO.[Pd]>[OH:8][CH2:9][C:10](=[O:19])[CH2:11][C:12]([O:14][C:15]([CH3:17])([CH3:16])[CH3:18])=[O:13]
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참가 물질

4

반응물 1

HCID 12035485Butanoic acid, 3-oxo-4-(phenylmethoxy)-, 1,1-dimethylethyl ester

생성물 1

HCID 13422882HCID 13422882, 화합물수율 65%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A mixture of 963 mg (5 mmol) of tert.-butyl 4-benzyloxyacetoacetate and 200 mg of palladium (10% on charcoal) in 50 ml of methanol was stirred at room temperature under a hydrogen atmosphere (1 atmosphere) for 1.5 hours. The catalyst was filtered off washed with a little methylene chloride. The filtrate solution was evaporated in vacuo and the residue was filtered through 3 g of neutral aluminum oxide (methylene chloride). The solvent was evaporated off in vacuo and the oil which remained was dried under a high vacuum. 567 mg (65% of tert.-butyl 4-hydroxyacetoacetate were obtained, and were used immediately for further reactions.

후처리

  1. filtrationThe catalyst was filtered off
  2. washwashed with a little methylene chloride
  3. customThe filtrate solution was evaporated in vacuo
  4. filtrationthe residue was filtered through 3 g of neutral aluminum oxide (methylene chloride)
  5. customThe solvent was evaporated off in vacuo
  6. customthe oil which remained was dried under a high vacuum

출처 및 근거

ORD 기록
ord-f51341f8d7fc416283fa878667acaac7
출처 데이터셋
uspto-grants-1986_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04616084

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