반응 #527700

반응 방정식

sodium carbonate

7-benzyloxy-1-[1-(2-chlorophenyl)cyclopropyl]-6-methoxy-3,4-dihydroisoquinoline

sodium tris[N-(2-methylpropyloxycarbonyl)prolyloxy]borohydride

sulphuric acid

→

7-benzyloxy-1-[1-(2-chlorophenyl)cyclopropyl]-6-methoxy-1,2,3,4-tetrahydroisoquinoline

용매

dichloromethane

dichloromethane

반응 조건

후처리

1. 1
   기타to reach ambient temperature
2. 2
   workup.STIRRINGstirring
3. 3
   workup.WAITcontinued for 1 hour
4. 4
   세척The organic layer was washed with brine
5. 5
   건조dried over magnesium sulphate
6. 6
   기타the solvent removed in vacuo

실험 절차

A solution of 7-benzyloxy-1-[1-(2-chlorophenyl)cyclopropyl]-6-methoxy-3,4-dihydroisoquinoline (0.5 g, prepared in a similar manner to that described in Example CA281) in dichloromethane (10 ml) was added dropwise at -40° C. to a stirred solution of sodium tris[N-(2-methylpropyloxycarbonyl)prolyloxy]borohydride (2.43 g) in dichloromethane (10 ml). The mixture was allowed to reach ambient temperature and was stirred for 49 hours. Dilute sulphuric acid (10 ml, 10% v/v) was added, and stirring continued for 1 hour. The mixture was basified by addition of saturated aqueous sodium carbonate solution. The organic layer was washed with brine, dried over magnesium sulphate and the solvent removed in vacuo to yield 7-benzyloxy-1-[1-(2-chlorophenyl)cyclopropyl]-6-methoxy-1,2,3,4-tetrahydroisoquinoline as a gum (0.42 g). This product was shown to have a 92% enantiomeric excess of one of the enantiomers.

출처