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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 983802생성일: 2026년 10월 25일

Triethylamine → 2-Hydroxy-N-methoxy-N-methyl-[1,1'-biphenyl]-3-carboxamide

https://huagongshe.com/reaction/983802

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-Phenylsalicylic acidHCID 9348—
반응물Oxalyl chlorideHCID 65578—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물2-Hydroxy-N-methoxy-N-methyl-[1,1'-biphenyl]-3-carboxamideHCID 1105431030.3%

반응 단계

2-hydroxy-3-phenylbenzoic acid (218, 3.0 g, 14 mmol) is dissolved in EtOAc (50 ml) and a few drops of DMF are added. Oxalyl chloride (2.5 ml, 1.5 eq) is added and the reaction is stirred under a dry atmosphere for 1 h. The reaction mixture is then concentrated in vacuo to yield a mixture of clear oil and white solid. This mixture is diluted with CH2Cl2 (50 ml) followed by the addition of N,O-dimethyl hydroxylamine hydrochloride (1.5 g, 1.1 eq) and triethylamine (3.9 ml, 2 eq). This mixture is stirred for 12-18 h under a dry atmosphere. Dilution of the reaction mixture with EtOAc and subsequent washing with dilute HCl and brine, followed by drying (MgSO4) and concentration in vacuo yields a mixture of reaction products. Flash chromatography (20/80 EtOAc/Hexanes) afforded N-methoxy-N-methyl-2-hydroxy-3-phenylbenzamide (219, 1.09 g) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06867200B1
출처 데이터셋uspto-grants-2005_03
ORD IDord-f276e7c9ffd34ec0ada420ba79622291
출처 메모uspto-grants-2005_03