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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1925707생성일: 2026년 10월 25일

Methyl 3-amino-2-thiophenecarboxylate → Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylate

https://huagongshe.com/reaction/1925707

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-amino-2-thiophenecarboxylateHCID 89652—
반응물4-t-Butylbenzenesulfonyl chlorideHCID 139882—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물Methyl 3-(4-tert-butylphenylsulfonamido)thiophene-2-carboxylateHCID 801564366%

반응 조건

온도40 °C

반응 단계

To a solution of methyl 3-aminothiophene-2-carboxylate (0.55 g; 3.5 mmol) in pyridine (2 mL) and dichloromethane (2 mL) was added 4-tert-butylbenzenesulfonyl chloride (0.98 g; 4.2 mmol). The resulting mixture was warmed to 40° C. to aid in solubility, then stirred at room temperature for 48 hours. The reaction mixture was diluted with dichloromethane and washed with aqueous hydrochloric acid (2N). The aqueous layer was separated and extracted with dichloromethane. The organic layers were combined, dried over anhydrous sodium sulfate, decanted, and filtered through a and of silica. The silica was washed with dichloromethane. The eluant was combined with hexanes and allowed to stand. After 24 hours the resulting solid product was collected by filtration to give the desired product as a white solid (817 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08178699B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-4fc1342cfdfe4611b700d4c23e1bcb89
출처 메모uspto-grants-2012_05