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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1839551생성일: 2026년 10월 25일

Triethylamine → 4-[2-Chloromethyl-4-phenyloxazol-5-yl]benzenesulfonamide

https://huagongshe.com/reaction/1839551

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Lithium ChlorideHCID 433294—
반응물4-[2-Hydroxymethyl-4-phenyloxazol-5-yl]benzenesulfonamideHCID 22246243—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-[2-Chloromethyl-4-phenyloxazol-5-yl]benzenesulfonamideHCID 22246345—

반응 단계

A solution of 4-[2-hydroxymethyl-4-phenyloxazol-5-yl]benzenesulfonamide (Step 2) (1.0 g, 3 mmol) and triethylamine (0.61 g, 6 mmol) was stirred in tetrahydrofuran (100 mL) at 0° C. Lithium chloride (0.25 g, 6 mmol) was added, followed by the dropwise addition of methanesulfonyl chloride (0.38 g, 3.3 mmol). After stirring for 3 h from 0° C. to 25° C., ethyl acetate (100 mL) was added, and the mixture was washed with 1N hydrochloric acid, brine and water, dried over magnesium sulfate, filtered, and concentrated. The crude product was purified by flash column chromatography on silica gel eluting with a 1:1 mixture of ethyl acetate: hexanes. The appropriate fractions were concentrated to a clear oil which solidified upon standing to give 4-[2-chloromethyl-4-phenyloxazol-5-yl]benzenesulfonamide as a white solid which was used in the next step without further purification or characterization.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06677364B2
출처 데이터셋uspto-grants-2004_01
ORD IDord-c3b8ce5af19c4468bc633cc2de318c48
출처 메모uspto-grants-2004_01