Potassium Hydroxide → HCID 68145100、化合物

反応式

C([O:4][C@H:5]1[CH2:9][CH2:8][C@@H:7]([CH:10]2[CH2:19][CH2:18][C:17]3[C:12](=[CH:13][CH:14]=[C:15]([O:20][CH3:21])[CH:16]=3)[CH2:11]2)[C@:6]1([CH3:26])[CH2:22][C:23]([OH:25])=[O:24])(=O)C.[OH-].[K+]>CO.O>[CH3:21][O:20][C:15]1[CH:16]=[C:17]2[C:12](=[CH:13][CH:14]=1)[CH2:11][CH:10]([C@H:7]1[C@:6]([CH3:26])([CH2:22][C:23]([OH:25])=[O:24])[C@@H:5]([OH:4])[CH2:9][CH2:8]1)[CH2:19][CH2:18]2

参加物

実験手順

To a solution of 3.33 g of (1S,2S,5S)-2-acetoxy-5-(1,2,3,4-tetrahydro-6-methoxy-2-naphthyl)-1-methylcyclo-pentaneacetic acid in 50 ml of methanol is added a solution of 3.00 g of potassium hydroxide in 15 ml of water. The resultant solution is refluxed for 2 hours, then diluted with 250 ml of water. Clarification is effected by filtration. The filtrate is acidified with hydrochloric acid. A solid precipitates which, isolated by filtration and recrystallized from a mixture of ethyl acetate and hexane, affords (1S,2S,5S)-5-(1,2,3,4-tetrahydro-6-methoxy-2-naphthyl)-2-hydroxy-1-methylcyclopentaneacetic acid melting at approximately 141.5°-142.5°. The product has a specific rotation of +65°.