반응 #96232

반응 방정식

dicyclohexylcarbodiimide

t-butanol

7-benzamido-3-methyl-3-cephem-4-carboxylic acid-1-oxide

→

t-butyl 7-benzamido-3-methyl-3-cephem-4-carboxylate-1-oxide

수율 48.0%

용매

dichloromethane

dichloromethane

반응 조건

후처리

1. 1
   기타the obtained N,N'-dicyclohexyl urea was separated by filtration
2. 2
   세척washed with dichloromethane
3. 3
   세척The combined filtrate and washing liquid
4. 4
   추출were extracted with a 2 N hydrochloric acid solution
5. 5
   기타The dichloromethane was evaporated under vacuo and toluene
6. 6
   workup.ADDITIONwas added to the residue
7. 7
   여과The obtained crystals were filtered off
8. 8
   세척were washed with toluene
9. 9
   기타After crystallization
10. 10
    workup.ADDITIONfrom a mixture of dichloromethane and toluene

실험 절차

A mixture of 103.2 g of dicyclohexylcarbodiimide, 43.5 g of t-butanol and 1.1 g of cuprous chloride was stored for 3 days at room temperature and the resulting compound was dissolved into 200 ml of dichloromethane. The solution was added dropwise to a stirred suspension of 35 g of 7-benzamido-3-methyl-3-cephem-4-carboxylic acid-1-oxide in 500 ml of dichloromethane and after stirring at room temperature for 24 hours, the obtained N,N'-dicyclohexyl urea was separated by filtration and washed with dichloromethane. The combined filtrate and washing liquid were extracted with a 2 N hydrochloric acid solution, a saturated sodium bicarbonate solution and twice with water. The dichloromethane was evaporated under vacuo and toluene was added to the residue. The obtained crystals were filtered off and were washed with toluene. After crystallization from a mixture of dichloromethane and toluene, 19.6 g of t-butyl 7-benzamido-3-methyl-3-cephem-4-carboxylate-1-oxide were obtained having the following characteristics:

출처