Isopropanol → 3-Hydroxyandrostane-17-carbonitrile
反応式
[C:1]([C@H:3]1[CH2:8][CH2:7][C@H:6]2[C@H:9]3[C@H:19]([CH2:20][CH2:21][C@:4]12[CH3:5])[C@:17]1([CH3:18])[C@H:12]([CH2:13][C:14](=[O:22])[CH2:15][CH2:16]1)[CH2:11][CH2:10]3)#[N:2].C(O)(C)C.C(N(CC)CC)C>O>[C:1]([C@H:3]1[CH2:8][CH2:7][C@H:6]2[C@H:9]3[C@H:19]([CH2:20][CH2:21][C@:4]12[CH3:5])[C@:17]1([CH3:18])[C@H:12]([CH2:13][C@H:14]([OH:22])[CH2:15][CH2:16]1)[CH2:11][CH2:10]3)#[N:2]参加物
実験手順
A solution of 17β-cyano-5α-androstan-3-one (1.0 g.) in the minimum volume of isopropanol (ca. 75 ml.) was added to a stock solution of chloroiridic acid/trimethyl phosphite complex (50 ml.) preneutralised to pH4 with triethylamine (4 ml.). This solution, after being refluxed for 20 hours, was poured into water (200 ml.) and extracted with chloroform. The chloroform solution was washed with water, dried (MgSO4), filtered and evaporated to a gum (1.13 g.). This was subjected to preparative t.l.c. eluting successively with ethanol/chloroform (1:49) and ethyl acetate/benzene (1:19). The main band was removed between the eluant change and the final elution was repeated four times before removing the main band. This gave pure title compound (195 mg.) as a white solid; m.p. 156°-159°; [α]D + 56° (c 0.4%).
後処理
- temperatureThis solution, after being refluxed for 20 hours
- extractionextracted with chloroform
- washThe chloroform solution was washed with water
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated to a gum (1.13 g.)
- washeluting successively with ethanol/chloroform (1:49) and ethyl acetate/benzene (1:19)
- customThe main band was removed between the eluant change
- washthe final elution
- custombefore removing the main band
- custom[α]D + 56° (c 0.4%)
出典と根拠
- ORDレコード
- ord-27f4976f2d5c4dda9bd01518dea0c083
- 出典データセット
- uspto-grants-1976_03
- 特許番号
- US03943124
反応ノート
読み込み中…