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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64957생성일: 2026년 10월 24일

Hydrochloric Acid → Methanesulfonylmethanesulfonyl chloride

https://huagongshe.com/ko/reaction/64957

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Phosphorus pentachlorideHCID 24819—
반응물Methanesulfinyl chlorideHCID 548463—
반응물Sodium (methylsulfonyl)methanesulfonateHCID 23721596—
용매Phosphorus oxychlorideHCID 24813—
생성물Methanesulfonylmethanesulfonyl chlorideHCID 556269—

반응 조건

온도70 °C

반응 단계

Phosphorus pentachloride (79.3 g, 0.381 mole) and sodium (methylsulfonyl)methanesulfonate (Formula II with Y=Na, X=H and R=CH3 ; 70 g, 0.359 mole) were stirred with 150 ml of phosphorus oxychloride. As the mixture was warmed to 70° C. in an oil bath, hydrogen chloride was slowly evolved, and the slurry thinned enough to be stirred with a magnetic stirrer. The mixture was heated for 18 hours in an oil bath at 80°-90° C., cooled, and filtered, and the residue was washed with dry chloroform. The chloroform caused the product to precipitate in the filtrate. The precipitate was collected, washed with a small amount of chloroform, and dried over sodium hydroxide pellets: yield, 28.5 g (41%); mp 109°-111° C.; MS (direct-probe temperature, 20° C.) m/e 193 (M+H), 192 (M), 177 (M-CH3), 157 (CH3SO2CH2SO2), 143, 141, 113 (CH2SO2Cl), 98 (CH3SOCl), 94, 93 (CH3SO2CH2), 79 (CH3SO2), 78, 64, 63 (CH3SO); IR (cm-1, strong and medium bands) 3045, 3025, 2995 s, 2930 s, 1405, 1390 s, 1380 s, 1360, 1335 s, 1325 sh, 1315 s, 1225, 1175 s, 1160 s, 1110 s, 980 s, 965, 860 s, 760 s, 695, 595 s, 515 s, 495 s, 460 s.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04611074
출처 데이터셋uspto-grants-1986_09
ORD IDord-78af65a9e00046378c37a31f1d69b2af
출처 메모uspto-grants-1986_09