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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37739생성일: 2026년 10월 23일

Thionyl Chloride → 4-Phenoxybenzene-1-sulfonyl chloride

https://huagongshe.com/ko/reaction/37739

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물4-phenoxybenzenesulfonic AcidHCID 11081501—
용매DimethylformamideHCID 6228—
생성물4-Phenoxybenzene-1-sulfonyl chlorideHCID 2794756—

반응 단계

The sulphonic acid (2a) was dissolved in an excess of thionyl chloride (30 mL), a catalytic amount of DMF (cat) was added, and the resulting mixture was stirred for 6 h at reflux. The solvent was evaporated and the residue dissolved in Et20 (40 mL). The ether solution was washed with 5% aqueous NaOH (3×40 mL) and water (6×40 mL), dried over anhydrous MgSO4, filtered, and concentrated in vacuo. After drying in high vacuum overnight, the pure product was obtained as a white solid. Yield 63%: 2.09 g, 7.44 mmol, (light yellow syrup). 1H-NMR (CDCl3): δ 7.44 (d, 3J=9.1 Hz, 2H, ArH), 7.38 (d, 3J=9.1 Hz, 2H, ArH), 7.19 (t, 1H, ArH), 7.12 (d, 3J=9.1 Hz, 2H, ArH), 6.98 (d, 3J=9.1 Hz, 2H, ArH)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524194B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-54b763fa48f0470b873aab1b94d435ed
출처 메모uspto-grants-2013_09