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

HRID 399674노트

반응식

HRID 399674 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+]>ClCl>[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 CH2 Cl2 (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-1d2158ac418e4872976c69654c9011c1
출처 데이터셋
uspto-grants-1998_10
특허 번호
US05821365

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