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12-fluoro-(Z)-3-dodecen-1-yl tetrahydropyranyl ether → 12-fluoro-(Z)-3-dodecen-1-ol

HRID 1263083
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HRID 1263083 반응식
O1CCCCC1[O:7][CH2:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][F:20]>CO>[F:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]/[CH:11]=[CH:10]\[CH2:9][CH2:8][OH:7]
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참가 물질

3

반응물 1

HCID 1337259212-fluoro-(Z)-3-dodecen-1-yl tetrahydropyranyl ether

생성물 1

HCID 8673950712-fluoro-(Z)-3-dodecen-1-ol수율 84.3%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
45 °C

실험 절차

To a solution of 12-fluoro-(Z)-3-dodecen-1-yl tetrahydropyranyl ether (0.5242 g, 1.83 mmol) (prepared as in Example 5 above) in methanol (10 ml) is added Dowex resin (0.5 g) and the mixture is heated at 45° C. overnight (Bongini et. al., Synthesis, 618, 1979). The resin is then filtered off and the solvent is removed in vacuo. The crude product is purified by flash chromatography using hexane/ethyl acetate (93:7, v/v) to give 12-fluoro-(Z)-3-dodecen-1-ol (312 mg, 83%) as a clear colorless oil: Rf=0.36, hexane/ethyl acetate (7:3, v/v); IR (film ν3100-3550 (OH), 3000 (C=CH); and H NMR (CDCl3) δ1.25-1.75 (m, 12H), 2.15 (m, 2H), 2.35 (br q, J=6 Hz, 2H), 3.65 (t, J=9 Hz, 2H), 4.41(dt, J=48 Hz, 6 Hz, 2H), 5.46 (m, 2H).

후처리

  1. custom(Bongini et. al., Synthesis, 618, 1979)
  2. filtrationThe resin is then filtered off
  3. customthe solvent is removed in vacuo
  4. customThe crude product is purified by flash chromatography

출처 및 근거

ORD 기록
ord-c5d003f873724ca6b7f3080bf1e4a7bc
출처 데이터셋
uspto-grants-1984_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04455441

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