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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393835생성일: 2026년 10월 24일

Triethylamine → 3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-[(4-nitrophenyl)methyl]-benzamide

https://huagongshe.com/ko/reaction/393835

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물3,5-Di-tert-butyl-4-hydroxybenzoic acidHCID 15007—
반응물4-Nitrobenzylamine hydrochlorideHCID 11252467—
용매TetrahydrofuranHCID 8028—
생성물3,5-bis-(1,1-dimethylethyl)-4-hydroxy-N-[(4-nitrophenyl)methyl]-benzamideHCID 2191855474%

반응 단계

1.88 g (10 mmoles) of p-nitrobenzylamine hydrochloride, 2.5 g (10 mmoles) of 3,5-di-tert-butyl-4-hydroxybenzoic acid, 1.38 ml (10 mmoles) of triethylamine and 2.26 g (11 mmoles) of dicyclohexylcarbodiimide are introduced into a 250 ml flask containing 25 ml of THF. The reaction medium is agitated for 15 hours at ambient temperature, the precipitate which appears is filtered out and rinsed with the minimum quantity of ethyl acetate. After concentration of the solution under reduced pressure, the residue is precipitated from a mixture of ethyl acetate/diethyl ether (1/4) and filtered. The crystals are washed abundantly with diethyl ether in order to finally produce, after drying, a white powder with a yield of 74% (2.85 g). Melting point: 230-231° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809088B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-99cb7217f35e4e9e8b18f6221e7d6561
출처 메모uspto-grants-2004_10