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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2447생성일: 2026년 10월 23일

Hydrochloric Acid → 4-Hydroxymethyl-N-(2-methoxyphenyl)benzenesulfonamide

https://huagongshe.com/ko/reaction/2447

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물4-((2-Methoxyphenyl)sulfamoyl)benzoic acidHCID 2333505—
반응물Sodium borohydrideHCID 4311764—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-Hydroxymethyl-N-(2-methoxyphenyl)benzenesulfonamideHCID 1968990869.6%

반응 단계

In an atmosphere of argon and with cooling in an ice bath, 4-[(2-methoxyanilino)sulfonyl]benzoic acid (150 mg, 0.488 mmol) was dissolved in THF (5 ml), to which were subsequently added dropwise triethylamine (0.14 ml, 1.0 mmol) and ethyl chloroformate (50 μl, 0.509 mmol). After 30 minutes of stirring at the same temperature, the thus formed precipitate was removed by filtration, and the resulting filtrate was concentrated. The thus obtained residue was dissolved in 5 ml of THF, and, with cooling in an ice bath, sodium borohydride (46.5 mg, 1.22 mmol) and water (1 ml) were added to the resulting solution. After 40 minutes of stirring at the same temperature, the reaction mixture was adjusted to pH 4 to 5 with 2N hydrochloric acid and extracted with ether. The organic layer was washed with saturated brine and dried on anhydrous magnesium sulfate. After removing the solvent by evaporation, the resulting colorless oily material was purified by silica gel column chromatography (ether) to obtain 99.6 mg (69.6%) of the title compound in the form of colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728835
출처 데이터셋uspto-grants-1998_03
ORD IDord-5fabbe4482ff451aa260f688512ff2dd
출처 메모uspto-grants-1998_03