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HCID 68379485, 화합물 → HCID 68379228, 화합물

HRID 1410062
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HRID 1410062 반응식
[CH3:1][C:2]1([CH3:27])[C:6]([CH3:8])([CH3:7])[O:5][B:4]([C:9]2[CH:10]=[C:11]([CH:24]=[CH:25][CH:26]=2)/[CH:12]=[CH:13]/[C:14]2[CH:23]=[CH:22][C:17]([C:18]([O:20][CH3:21])=[O:19])=[CH:16][CH:15]=2)[O:3]1>CO.O=[Pt]=O>[CH3:7][C:6]1([CH3:8])[C:2]([CH3:1])([CH3:27])[O:3][B:4]([C:9]2[CH:10]=[C:11]([CH:24]=[CH:25][CH:26]=2)[CH2:12][CH2:13][C:14]2[CH:15]=[CH:16][C:17]([C:18]([O:20][CH3:21])=[O:19])=[CH:22][CH:23]=2)[O:5]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68379485HCID 68379485, 화합물

생성물 1

HCID 68379228HCID 68379228, 화합물수율 50%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 887Methanol용매

실험 절차

A mixture of (E)-methyl 4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)styryl)benzoate (200 mg, 0.55 mmol) and PtO2 (50 mg, 0.22 mmol) in 30 mL of MeOH was stirred at room temperature for 18 hours under H2 atmosphere. The solvent was evaporated and the residue was purified by silica gel chromatography (200-300 mesh, eluting with a mixture of petroleum ether and ethyl acetate=50:1) to give methyl 4-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)benzoate (90 mg, 50%) as a colorless oil

후처리

  1. customThe solvent was evaporated
  2. customthe residue was purified by silica gel chromatography (200-300 mesh
  3. washeluting with a mixture of petroleum ether and ethyl acetate=50:1)

출처 및 근거

ORD 기록
ord-c1de6794473a4289b4f6524b40cf94a3
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08921383B2

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