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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1741865생성일: 2026년 10월 26일

Thiophene-3-carboxylic acid → 4-Ethyl-2-propyl-1-(3-thenoyl) semicarbazide

https://huagongshe.com/reaction/1741865

반응식

참여 물질

역할이름HCID투입량
반응물Thiophene-3-carboxylic acidHCID 6918—
반응물TriethylamineHCID 8471—
반응물Isobutyl chloroformateHCID 62365—
반응물4-Ethyl-2-propyl semicarbazideHCID 19010929—
용매TetrahydrofuranHCID 8028—
생성물4-Ethyl-2-propyl-1-(3-thenoyl) semicarbazideHCID 54099638—

반응 조건

온도5 °C

반응 단계

A stirred solution of 2.62 g (20.5 mmol) of thiophene-3-carboxylic acid and 2.8 mL (20.0 mmol) of triethylamine in 20 mL of THF was cooled to 5° C. and 2.6 mL (20.0 mmol) of isobutyl chloroformate was added dropwise over 5 minutes. The mixture was stirred at 5° C. for 5 minutes and added to a suspension of the 4-ethyl-2-propyl semicarbazide prepared above in 20 mL of THF at 5° C. This mixture was allowed to warm to room temperature and stirred overnight. The mixture was concentrated to remove most of the solvent, taken up in 75 mL of water and extracted with two 100 mL portions of ethyl acetate. The combined ethyl acetate extracts were washed with 50 mL of 5% aqueous HCl and 50 mL of saturated aqueous sodium bicarbonate (NaHCO3), and dried over MgSO4. Removal of the solvent left 5.30 g of crude 4 -ethyl-2-propyl-1-(3-thenoyl) semicarbazide as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05334726
출처 데이터셋uspto-grants-1994_08
ORD IDord-3788da22400547588000d5e5ed67015c
출처 메모uspto-grants-1994_08