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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1290699생성일: 2026년 10월 25일

Diphenyl Ether → 4-phenoxybenzenesulfonic Acid

https://huagongshe.com/reaction/1290699

반응식

참여 물질

역할이름HCID투입량
반응물Diphenyl EtherHCID 7583—
반응물2,2,4-TrimethylpentaneHCID 10907—
반응물Chlorosulfonic acidHCID 24638—
용매DichloromethaneHCID 6344—
생성물4-phenoxybenzenesulfonic AcidHCID 11081501110.3%

반응 단계

To a stirred solution of 42.5 g (0.25 mol) of phenyl ether in 200 mL of dichloromethane at -20° C. under argon was slowly added 23.3 g (0.20 mol) of chlorosulfonic acid. After the addition was complete, the reaction was allowed to slowly warm to room temperature. After 16 h, 150 mL of isooctane was added and the solution was concentrated to an oily residue. Redissolution in 200 mL of 1:3 dichloromethane/isooctane and reconcentration with cooling to about 100 mL gave a solid. The supernatant was decanted, and the solid triturated with additional isooctane and then dried in vacuo to give 55.2 g of crude 4-phenoxybenzene sulfonic acid. The crude acid was dissolved in 200 mL of dichloromethane, and 34 g (0.25 mol) of oxalyl chloride was added, followed by 2.5 mL of DMF. After 2 days, the reaction solution was poured into 200 mL of ice water, and extracted with 400 mL of hexane. The organic layer was washed with 100 mL of water and 100 mL of brine, dried over magnesium sulfate, and concentrated. Recrystallization of the residue from dichloromethane/isooctane gave 38.5 g of 4-phenoxybenzenesulfonyl chloride as a white solid: mp 41.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05753653
출처 데이터셋uspto-grants-1998_05
ORD IDord-475b41f4e2294849a96c990724c74fea
출처 메모uspto-grants-1998_05