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HCID 89581294, 화합물 → HCID 89580553, 화합물

HRID 1501170
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HRID 1501170 반응식
[O:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[CH:18]=[CH:17][C:9]([C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])=[CH:8][CH:7]=1>CO.[Pd]>[O:1]1[CH2:5][CH2:4][CH2:3][CH:2]1[C:6]1[CH:18]=[CH:17][C:9]([C:10]([O:12][C:13]([CH3:14])([CH3:16])[CH3:15])=[O:11])=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 89581294HCID 89581294, 화합물

생성물 1

HCID 89580553HCID 89580553, 화합물수율 86%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of tert-butyl 4-(furan-2-yl)benzoate (400 mg, 1.64 mmol) in methanol (20 mL) was added palladium on carbon (10%, 100 mg). After stirring for 24 hours at room temperature under hydrogen atmosphere, the mixture was filtered. And the filtrate was concentrated in vacuo to give tert-butyl 4-(tetrahydrofuran-2-yl)benzoate (350 mg, 86%) as a white solid. LRMS (M+H+) m/z: calcd 248.14. found 248. 1H NMR (300 MHz, CD3OD): δ 7.94-7.85 (m, 2H), 7.44-7.28 (m, 2H), 4.95-4.93 (m, 1H), 3.60-3.56 (m, 2H), 2.73-2.68 (m, 2H), 1.77-1.73 (m, 2H), 1.68 (s, 9H).

후처리

  1. filtrationthe mixture was filtered
  2. concentrationAnd the filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-5853d2e6105c42ff9c71d40ba4770e76
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09206128B2

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