돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51189생성일: 2026년 10월 24일

Hydrochloric Acid → Bis(4-n-butylcyclohexylsulfonyl)diazomethane

https://huagongshe.com/ko/reaction/51189

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물p-Toluenesulfonyl azideHCID 13661—
반응물Bis(4-n-butylcyclohexylsulfonyl)methaneHCID 22737628—
용매DichloromethaneHCID 6344—
생성물Bis(4-n-butylcyclohexylsulfonyl)diazomethaneHCID 2273764920.6%

반응 단계

In 91 g of dichloromethane were dissolved 10.5 g (0.025 mol) of the bis(4-n-butylcyclohexylsulfonyl)methane prepared above and 7.5 g (0.038 mol) of p-toluenesulfonylazide. The solution was cooled on an ice bath, to which 3.7 ml (0.0025 mol) of diazabicyclo[5.4.0]-7-undecene (DBU) was added dropwise at a temperature below 5° C. The solution was ripened at the temperature for 15 minutes, after which 38 g of water and 10 g of 12N conc. hydrochloric acid were added. The organic layer was separated and washed with 50 g of water. The solvent was distilled off in vacuum, leaving an oily matter. It was purified by silica gel column chromatography (using dichloromethane as a developing solvent), obtaining 2.3 g of the desired bis(4-n-butylcyclohexylsulfonyl)diazomethane. The yield was 20%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713612B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-710f2b20ca6b4f8b8c10f43115d88589
출처 메모uspto-grants-2004_03