Benzyl Bromide → (1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol

HRID 2360264

반응식

HRID 2360264 반응식
[C@@H:1]12[CH2:8][C@@H:4]([C@@H:5]([OH:7])[CH2:6]1)[CH2:3][C@@H:2]2[OH:9].C1OCCOCCOCCOCCOC1.O1CCCC1.[OH-].[Na+].Br[CH2:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>>[CH2:33]([O:7][C@H:5]1[CH2:6][C@H:1]2[CH2:8][C@@H:4]1[CH2:3][C@@H:2]2[OH:9])[C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1

참가 물질

6

반응물 5

HCID 7498Benzyl BromideHCID 8028TetrahydrofuranHCID 14798Sodium HydroxideHCID 3633615-Crown-5HCID 9989289(1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diol

생성물 1

HCID 10036335(1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol

반응 조건

온도
10 °C

실험 절차

To a stirred solution of (1R,2S,4R,5S)-bicyclo[2.2.1]-heptane-2,5-diol (1.15 g, 8.97 mmol) and 15-crown-5 (0.054 mL, 0.269 mmol) in tetrahydrofuran (30.0 mL, 8.97 mmol) were added at 10° C. (ice/water bath) finely ground sodium hydroxide (2.15 g, 53.8 mmol) and 1-(bromomethyl)benzene (1.07 mL, 8.97 mmol). After stirring at 10° C. for 3 h, the mixture was stirred at ambient temperature overnight. The mixture was partitioned between EtOAc and water, and the organic portions were washed with brine, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 80% of ethyl acetate in hexanes). The title compound was obtained as a colorless oil.

후처리

  1. stirringthe mixture was stirred at ambient temperature overnight
  2. customThe mixture was partitioned between EtOAc and water
  3. washthe organic portions were washed with brine
  4. customThe crude product was purified by flash column chromatography (0 to 80% of ethyl acetate in hexanes)

출처 및 근거

ORD 기록
ord-6a53e48d1cd7428eb757d87955dad714
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08686011B2

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