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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 975324생성일: 2026년 10월 24일

Phenethylamine → 4-((2-Phenylethyl)aminocarbonyl)benzenesulfonamide

https://huagongshe.com/ko/reaction/975324

반응식

참여 물질

역할이름HCID투입량
반응물PhenethylamineHCID 1001—
반응물TriethylamineHCID 8471—
반응물CarzenideHCID 8739—
반응물Ethyl chloroformateHCID 10928—
용매TetrahydrofuranHCID 8028—
생성물4-((2-Phenylethyl)aminocarbonyl)benzenesulfonamideHCID 1997074867%

반응 조건

온도-10 °C

반응 단계

20.1 g (0.1 mol) of 4-carboxybenzenesulfonamide were suspended in 300 ml of anhydrous tetrahydrofuran and treated dropwise at 0° C. with stirring with 15.2 ml (0.11 mol) of triethylamine. After 30 min, 10.5 ml (0.11 mol) of ethyl chloroformate were added dropwise at 0° C., the mixture was stirred at this temperature for 1 h, cooled to -10° C. and 12.1 g (0.1 mol, 12.5 ml) of 2-phenylethylamine in 30 ml of anhydrous tetrahydrofuran were added dropwise. After 1 h at 0° C., the mixture was warmed to 20° C. and concentrated in vacuo, the solid residue was treated with water, filtered off with suction and recrystallized from ethanol, and 20.4 g of product were obtained, M.p. 243°-245° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05607954
출처 데이터셋uspto-grants-1997_03
ORD IDord-b4596b61bc464c4a8bfb016e889acaa6
출처 메모uspto-grants-1997_03