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

HRID 1107008ノート

反応式

HRID 1107008 の反応式
[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

参加物

7

実験手順

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.

後処理

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

出典と根拠

ORDレコード
ord-f5a310ece8194130aeddc9db49eae592
出典データセット
uspto-grants-2000_05
特許番号
US06057440

反応ノート

読み込み中…