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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Triethylsiloxy-4-trifluoromethyl-2,5-cyclohexadien-1-one → 4-Triethylsiloxy-4-trifluoromethylcyclohexanone

HRID 1382013
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HRID 1382013 반응식
[CH2:1]([Si:3]([CH2:18][CH3:19])([CH2:16][CH3:17])[O:4][C:5]1([C:12]([F:15])([F:14])[F:13])[CH:10]=[CH:9][C:8](=[O:11])[CH:7]=[CH:6]1)[CH3:2].[H][H]>C(O)C.[Pd]>[CH2:16]([Si:3]([CH2:1][CH3:2])([CH2:18][CH3:19])[O:4][C:5]1([C:12]([F:14])([F:13])[F:15])[CH2:6][CH2:7][C:8](=[O:11])[CH2:9][CH2:10]1)[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 143434944-Triethylsiloxy-4-trifluoromethyl-2,5-cyclohexadien-1-oneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 200620264-Triethylsiloxy-4-trifluoromethylcyclohexanone

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A solution of 291 mg of 4-triethylsiloxy-4-trifluoromethyl-2,5-cyclohexadien-1-one in 2 mL of absolute ethanol was treated with a few mg of 5% palladium on carbon, hydrogenated in a Parr shaker for one hour under 50 psig of hydrogen, and filtered. Concentration of the filtrate gave 4-triethylsiloxy-4-trifluoromethylcyclohexanone: 1H NMR (CDCl3)δ0.45-1.16 (m, 15H), 1.92-2.89 (m, 8H); mass spectrum (70 eV) m/z (relative intensity) 267 (19, M-C2H5), 115 (45), 105 (33), 87 (100), 81 (22), 77 (67), 73 (20), 67 (29), 59 (57), 55 (84), 47 (20).

후처리

  1. filtrationfiltered

출처 및 근거

ORD 기록
ord-fb6a904b1ca9416093946a0785ffe933
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04804773

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