반응 #929061

반응 방정식

Trimethyloxonium tetrafluoroborate

1-(tert-butoxycarbonyl)hexahydro-(5H)-1,4-diazepin-5-one

→

1-(tert-butoxycarbonyl)-2,3,6,7-tetrahydro-5-methoxy-(1H)-1,4-diazepine

수율 85.0%

용매

methylene chloride

반응 조건

후처리

1. 1
   기타The reaction mixture was partitioned between 10 mL of saturated aqueous sodium bicarbonate and 20 mL of ethyl acetate
2. 2
   기타The organic layer was separated
3. 3
   추출the aqueous layer was extracted with 3×10 mL of ethyl acetate
4. 4
   세척The combined ethyl acetate layers were washed with saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride
5. 5
   건조After drying over anhydrous sodium sulfate
6. 6
   농축the organic solution was concentrated in vacuo

실험 절차

Trimethyloxonium tetrafluoroborate (Meerwein's salt) (141 mg, 0.94 mmol) was added in one portion to a solution of 1-(tert-butoxycarbonyl)hexahydro-(5H)-1,4-diazepin-5-one (200 mg, 0.94 mmol) in 2.0 mL of anhydrous methylene chloride. The mixture was stirred overnight at room temperature. The reaction mixture was partitioned between 10 mL of saturated aqueous sodium bicarbonate and 20 mL of ethyl acetate. The organic layer was separated and the aqueous layer was extracted with 3×10 mL of ethyl acetate. The combined ethyl acetate layers were washed with saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride. After drying over anhydrous sodium sulfate, the organic solution was concentrated in vacuo to give 180 mg (85%) of 1-(tert-butoxycarbonyl)-2,3,6,7-tetrahydro-5-methoxy-(1H)-1,4-diazepine as a yellow liquid.

출처