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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1737450생성일: 2026년 10월 27일

N-Methylphenylethanolamine → N-(2-hydroxy-2-phenylethyl)-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/1737450

반응식

참여 물질

역할이름HCID투입량
반응물N-MethylphenylethanolamineHCID 913—
반응물Benzenesulfonyl chlorideHCID 7369—
반응물DiisopropylethylamineHCID 81531—
용매TetrahydrofuranHCID 8028—
생성물N-(2-hydroxy-2-phenylethyl)-N-methylbenzenesulfonamideHCID 21842621—

반응 단계

A solution of α-(methylaminomethyl)benzyl alcohol (1.00 g, 6.61 mmol) in 15 mL of THF was cooled in an ice bath. Benzenesulfonyl chloride (0.886 mL, 1.23 g, 6.94 mmol) and N,N-diisopropylethylamine (2.3 mL, 1.7 g, 13 mmol) were added and mixture was allowed to warm to room temperature. After 30 min, the solvent was evaporated and the residue was partitioned between 50 mL of ethyl acetate and 40 mL of saturated aqueous sodium bicarbonate. The aqueous layer was extracted with 2×50 mL of ethyl acetate. The combined organic layers were washed with 50 mL of brine, dried over sodium sulfate, and evaporated. Purification by flash column chromatography on silica gel, eluting with 20-50% ethyl acetate in hexane, gave the title compound in quantitative yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05962462
출처 데이터셋uspto-grants-1999_10
ORD IDord-ba598985bff041bf90162b74bd66b628
출처 메모uspto-grants-1999_10