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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl acetate hexane → HCID 22161963, 화합물

HRID 1088727
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HRID 1088727 반응식
[CH2:1]([C:4]1[CH:12]=[CH:11][C:7]2[CH2:8][CH2:9][S:10][C:6]=2[CH:5]=1)[CH:2]=[CH2:3].CCCCCC.CCOC(C)=O>C(O)C.[Pd]>[CH2:1]([C:4]1[CH:12]=[CH:11][C:7]2[CH2:8][CH2:9][S:10][C:6]=2[CH:5]=1)[CH2:2][CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 21226206Ethyl acetate hexaneHCID 22161965HCID 22161965, 화합물

생성물 1

HCID 22161963HCID 22161963, 화합물수율 85.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution of 6-allyl-2,3-dihydrobenzothiophene (95 mg, 0.49 mmole) in 10 mL absolute ethanol was hydrogenated at 40 psi over 20 mg 10% Pd/C at room temperature overnight. TLC (90/10, hexane/EtOAc) indicated the reaction to be complete. The catalyst was filtered off through a celite pad and the filtrate concentrated down to afford 96 mg crude product as an oil. Purification by flash chromatography (90/10, hexane/EtOAc) afforded 75 mg white solids mp 58°-60° C. (78%).

후처리

  1. customthe reaction
  2. filtrationThe catalyst was filtered off through a celite pad
  3. concentrationthe filtrate concentrated down
  4. customto afford 96 mg crude product as an oil
  5. customPurification by flash chromatography (90/10, hexane/EtOAc)

출처 및 근거

ORD 기록
ord-840ed4cbd7704e2b8c2f736bd95d9421
출처 데이터셋
uspto-grants-1990_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04963580

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