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3-(1,3-Benzodioxol-5-yl)prop-2-yn-1-ol → HCID 11608001, 화합물

HRID 1008759
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HRID 1008759 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]#[C:11][CH2:12][OH:13])=[CH:9][C:4]=2[O:3][CH2:2]1>C(Cl)Cl.O=[Mn]=O>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]#[C:11][CH:12]=[O:13])=[CH:9][C:4]=2[O:3][CH2:2]1
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참가 물질

4

반응물 1

HCID 111376463-(1,3-Benzodioxol-5-yl)prop-2-yn-1-ol

생성물 1

HCID 11608001HCID 11608001, 화합물수율 51.6%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of 3-(1,3-benzodioxol-5-yl)prop-2-yn-1-ol (242 mg, 1.37 mmol, obtained as described in Nugent et al., 1987, J. Am. Chem. Soc., 109, 2788) in anhydrous DCM (12 mL) was added MnO2 (2.70 g, 31.1 mmol) portion wise over 2 h. The resulting mixture was stirred at rt for one additional hour, then filtered on a bed of Celite and the filtrates were evaporated under reduced pressure to give 123 mg (51%) of the title compound as a brown solid. HPLC, Rt: 2.76 min (purity: 98.9%). 1H NMR (CDCl3) δ: 9.37 (s, 1H), 7.18 (m, 1H), 7.00 (m, 1H), 6.82 (d, J=8.3 Hz, 1H), 6.03 (s, 2H).

후처리

  1. filtrationfiltered on a bed of Celite
  2. customthe filtrates were evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-8621e4d42ddc4b878576e4219ab31fc7
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07973039B2

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