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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 236532생성일: 2026년 10월 25일

Butyl isocyanate → N-(Butylcarbamoyl)-3-methylthiophene-2-sulfonamide

https://huagongshe.com/reaction/236532

반응식

참여 물질

역할이름HCID투입량
반응물Butyl isocyanateHCID 8110—
반응물Potassium CarbonateHCID 11430—
반응물3-Methylthiophene-2-sulfonamideHCID 341083—
용매AcetoneHCID 180—
생성물N-(Butylcarbamoyl)-3-methylthiophene-2-sulfonamideHCID 13203354—

반응 단계

To 150 ml of acetone and 3-methyl-2-thiophenesulfonamide was added 11 g of n-butyl isocyanate and 14 g of anhydrous potassium carbonate. After stirring at ambient temperature for 24 hours, the mixture was concentrated to 2/3 of its volume and poured into ice-water. The pH was adjusted to 3 by the addition of hydrochloric acid and the solid thus obtained was filtered, air dried and triturated with 1-chlorobutane to yield 10.6 g of N-(butylaminocarbonyl)-3-methyl-2-thiophenesulfonamide melting at 144°-146°. It showed absorption peaks by NMR (60 MC) at 2.6 δ (singlet, CH3), 1-1.8 δ (mult., C3H7), 3.42 δ (trip., N--CH2 --of butyl) and at 7.1 δ and 7.7 δ (2 doublets for CH's of thiophene) consistent for the desired structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04645529
출처 데이터셋uspto-grants-1987_02
ORD IDord-dc01c366dd624bb48a108c0d84c51912
출처 메모uspto-grants-1987_02