돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2210996생성일: 2026년 10월 26일

Thionyl Chloride → N,N-Diethyl-2-phenylnaphtho[1,2-d][1,3]oxazole-5-sulfonamide

https://huagongshe.com/reaction/2210996

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물pyridinium 3-hydroxy-4-(N-benzoylamino)-1-naphthalenesulfonateHCID 19378056—
용매TolueneHCID 1140—
생성물N,N-Diethyl-2-phenylnaphtho[1,2-d][1,3]oxazole-5-sulfonamideHCID 371523881.6%

반응 단계

A mixture of 3.43 g pyridinium 3-hydroxy-4-(N-benzoylamino)-1-naphthalenesulfonate and 10 ml thionyl chloride was refluxed for 3.5 hours. Toluene (20 ml) was added and the excess thionyl chloride was distilled off with toluene under reduced pressure. The solid residue was dissolved in 50 ml methylene chloride and 10 ml diethylamine was added portionwise while stirring. After 30 min, the reaction mixture was poured into 100 ml ice-water and extracted with 100 ml dichloromethane. The organic phase was separated, washed with water, and dried over sodium sulfate. Evaporation of the solvent gave 2.52 g N,N-diethyl-2-phenylnaphth[1,2-d]oxazole-5-sulfonamide of high purity by NMR. Recrystallization from 95% ethanol gave an analytical sample, m.p. 157° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05461155
출처 데이터셋uspto-grants-1995_10
ORD IDord-48ba579d39f44eed80357b9ea8c56394
출처 메모uspto-grants-1995_10