Hydrochloric Acid → (3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindol-4-ol hydrochloride
反応式
[ClH:1].[C:2]1([C:8]2([C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)[C@@H:16]3[C@@H:12]([CH2:13][N:14](C(OC(C)(C)C)=O)[CH2:15]3)[C@@:11]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=3[O:31][CH3:32])([OH:24])[CH2:10][CH2:9]2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>O1CCOCC1>[ClH:1].[C:33]1([C:8]2([C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[C@@H:16]3[C@@H:12]([CH2:13][NH:14][CH2:15]3)[C@@:11]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=3[O:31][CH3:32])([OH:24])[CH2:10][CH2:9]2)[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1参加物
4
実験手順
A solution of 100 cm3 of a 5.2N solution of hydrochloric acid in dioxane is added at room temperature to a solution of 7.63 g of (3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)-2-(tert-butoxycarbonyl)perhydroisoindol-4-ol in 66 cm3 of dioxane. The reaction mixture is stirred for 1 hour at this temperature and then concentrated to dryness under reduced pressure (2.7 kPa). The residue is washed with acetonitrile, filtered off and then dried. There are obtained 4.88 g of (3aS,4S,7aS)-7,7-diphenyl-4-(2-methoxyphenyl)perhydroisoindol-4-ol hydrochloride in the form of white crystals melting at 271° C. (Maquenne block).
後処理
- concentrationconcentrated to dryness under reduced pressure (2.7 kPa)
- washThe residue is washed with acetonitrile
- filtrationfiltered off
- customdried
出典と根拠
- ORDレコード
- ord-18f4cb94cc744781aac76efa6504b632
- 出典データセット
- uspto-grants-2001_01
- 特許番号
- US06177450B1
反応ノート
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