Hydrochloric Acid → HCID 67736920、化合物
反応式
[ClH:1].[C:2]1([C@:8]2([OH:36])[CH2:16][CH2:15][C:14]([C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C@@H:13]3[C@H:9]2[CH2:10][N:11](C(OC(C)(C)C)=O)[CH2:12]3)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>O1CCOCC1>[ClH:1].[C:2]1([C@:8]2([OH:36])[CH2:16][CH2:15][C:14]([C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)([C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=3)[C@@H:13]3[C@H:9]2[CH2:10][NH:11][CH2:12]3)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
4
実験手順
115 cm3 of a 6.3N solution of hydrochloric acid in dioxane are added to a solution of 6.8 g of (3aS,4S,7aS)-4,7,7-triphenyl-2-tert-butoxycarbonylperhydroisoindol-4-ol in 60 cm3 of dioxane at room temperature. The reaction mixture is stirred at this temperature for 2 hours and then concentrated to dryness under reduced pressure (2.7 kPa). The residue is washed with acetonitrile, filtered off and then dried. 4 g of (3aS,4S,7aS)-4,7,7-triphenylperhydroisoindol-4-ol hydrochloride are obtained in the form of a white foam.