Hydrochloric Acid → (+/-)-3-(Benzyloxy)methyl-1,6hexanediol

HRID 55442노트

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HRID 55442 반응식
[O:1]=[O+][O-].[CH2:4]([O:11][CH:12]=[C:13]1[CH2:18][CH2:17]C[CH:15]=[CH:14]1)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.CSC.B.Cl.[C:24]([O-:27])(O)=O.[Na+]>C(Cl)Cl>[CH2:4]([O:11][CH2:12][CH:13]([CH2:18][CH2:17][CH2:24][OH:27])[CH2:14][CH2:15][OH:1])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1

참가 물질

7

실험 절차

Ozone was bubbled through a solution of (±)-3-benzyloxymethylene-1-cyclohexene (1.35 g, 6.70 mmol) in CH2Cl2 (65 mL) at -78° C. until the blue color of unreacted ozone persisted. The reaction mixture was allowed to warm to room temperature, while dry nitrogen was bubbled through the reaction. Borane-dimethyl sulfide complex (10.0M in THF, 2.7 mL, 27.8 mmol) was added via syringe over several minutes, and the reaction mixture was allowed to stand at room temperature for 24 hours. The reaction mixture was treated with 5 percent aqueous HCl (1 mL) and stirred vigorously for one hour. Solid NaHCO3 was added until the mixture tested basic to litmus paper. The mixture was dried over anhydrous MgSO4. The reaction mixture was filtered and concentrated to afford the crude (±)-3-(benzyloxy)methyl-1,6 hexanediol (1.49 g, ca. 100 percent) as an oil. This material, which showed essentially a single spot on TLC analysis, Rf=0.25, 25 percent EtOAc in hexane, was used directly in the next step without further purification.

후처리

  1. customwas bubbled through the reaction
  2. dry with materialThe mixture was dried over anhydrous MgSO4
  3. filtrationThe reaction mixture was filtered
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9b6cd5d4179a407c8bff138138fead4e
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05624949

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