反応式
C[O:2][C:3]([C:5]1([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]1)=O.[H-].[H-].[H-].[H-].[Li+].[Al+3].C1(C2(CO)CCCC2)C=CC=CC=1>>[C:11]1([C:5]2([CH2:3][OH:2])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6]2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1参加物
4
実験手順
This compound was prepared (1.02 g, 5.43 mmol, 62%) from the product of Step B (1.91 g, 8.76 mmol) using LiAlH4 (0.75 g, 37.95 mmol) according to the procedure for synthesizing 1-phenylcyclopentanemethanol set forth in Step B, Example 1, with the exception that this compound precipitated out of solution following the steps of: (a) destroying the excess hydride; (b) separating the aluminum salts by filtration; and (c) washing with water (3×4 mL in this Example). Filtration of the precipitate gave 1-phenylcyclohexanemethanol as a white solid, mp 63°-64° C. (compared with reported value, J. Org. Chem. 27:3434 (1962), of 63°-64° C.).
後処理
- customprecipitated out of solution
- customdestroying the excess hydride
- custom(b) separating the aluminum salts
- filtrationby filtration
- washand (c) washing with water (3×4 mL in this Example)
- filtrationFiltration of the precipitate
出典と根拠
- ORDレコード
- ord-0fd12617cab34d8cae6425175de8170b
- 出典データセット
- uspto-grants-1994_07
- 特許番号
- US05331010
関連ノート
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