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6-Chloro-1-hexanol → (3R,3aR,6R,6aR)-6-hydroxyhexahydrofuro[3,2-b]furan-3-yl 6-chlorohexyl carbonate

HRID 1676014
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HRID 1676014 반응식
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][OH:8].[C:9](=O)([O:20]C1C=CC([N+]([O-])=O)=CC=1)[O:10][C@@H:11]1[CH2:15][O:14][C@@H:13]2[C@H:16]([OH:19])[CH2:17][O:18][C@H:12]12>CN(C)C1C=CN=CC=1.C(Cl)Cl>[C:9](=[O:20])([O:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][Cl:1])[O:10][C@@H:11]1[CH2:15][O:14][C@@H:13]2[C@H:16]([OH:19])[CH2:17][O:18][C@H:12]12
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HCID 748286-Chloro-1-hexanolHCID 58209393(3R,3aR,6R,6aR)-6-hydroxyhexahydrofuro[3,2-b]furan-3-yl 4-nitrophenyl carbonate2회

생성물 1

HCID 59509509(3R,3aR,6R,6aR)-6-hydroxyhexahydrofuro[3,2-b]furan-3-yl 6-chlorohexyl carbonate

시약·촉매·용매 2

HCID 142844-(Dimethylamino)pyridine촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of (3R,3aR,6R,6aR)-6-hydroxyhexahydrofuro[3,2-b]furan-3-yl 4-nitrophenyl carbonate (1.13 g, 3.63 mmol) in DCM (15 ml), (prepared as described in EXAMPLE 7, Step C), 6-chlorohexanol (596 mg, 4.36 mmol) and 4-dimethylaminopyridine (89 mg, 0.73 mmol) were added and the mixture was stirred at room temperature for 18 hrs. Then the mixture was diluted with DCM and washed with a 5% solution of sodium dihydrogen phosphate (20 ml). The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (Biotage SP1, EtOAc/n-hexane from 12 to 80%), affording the title compound as colorless oil.

후처리

  1. washwashed with a 5% solution of sodium dihydrogen phosphate (20 ml)
  2. dry with materialThe organic layer was dried over sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by flash chromatography (Biotage SP1, EtOAc/n-hexane from 12 to 80%)

출처 및 근거

ORD 기록
ord-ce6e0a7cb6a84034b4b1b37ffda40aad
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08003811B2

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