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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583134생성일: 2026년 10월 24일

Triethylamine → N-(3-methylpent-1-yn-3-yl)-4-nitrobenzamide

https://huagongshe.com/ko/reaction/583134

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Nitrobenzoyl chlorideHCID 8502—
반응물3-Methyl-1-pentyn-3-amine hydrochlorideHCID 12232990—
용매DichloromethaneHCID 6344—
생성물N-(3-methylpent-1-yn-3-yl)-4-nitrobenzamideHCID 15405291—

반응 단계

In a three-necked, round-bottomed flask fitted with a mechanical stirrer, nitrogen inlet and thermometer were placed 4 grams (g) (0.03 mole) of 3-amino-3-methyl-1-pentyne hydrochloride (4 grams (g) (0.03 mole) suspended in 100 milliliters (mL) of methylene chloride in a three-necked, round-bottomed flask fitted with a mechanical stirrer, nitrogen inlet and thermometer. Triethylamine (6.82 g, 9.4 mL) was added slowly, keeping the temperature between 5° C. and 10° C. 4-nitrobenzoyl chloride 5 g (0.027 mole) was added to the resulting mixture at a rate to keep the reaction temperature between 5° C. and 10° C. After the addition was complete the reaction mixture was stirred at room temperature for 0.5 hours, and was then sequentially washed with water (2×100 mL), 5% aqueous hydrochloric acid, (2×100 mL), water (1×50 mL), 5% aqueous sodium hydroxide (2×100 mL) and finally with water (1×100 mL) before being dried over anhydrous magnesium sulfate. The solvent was removed in the rotary evaporator, yielding N-(3-methylpent-1-yn-3-yl)-4-nitrobenzamide, used as such in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05929098
출처 데이터셋uspto-grants-1999_07
ORD IDord-3462e37789814c90a554d3fd75a977c8
출처 메모uspto-grants-1999_07