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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3926생성일: 2026년 10월 24일

Sodium hydride → Nicotinic Acid

https://huagongshe.com/ko/reaction/3926

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물SodiumHCID 5360545—
반응물tetrahydrofuran N,N-dimethylformamideHCID 21974620—
반응물pyridine-4-thiolHCID 178418431—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Nicotinic AcidHCID 938—

반응 단계

5.2 g of 90% pyridinium bromide perbromide was added in one portion to a solution of 5 g of 3-pyridinecarboxylic acid, 5-cyano-1,4-dihydro-2,6-dimethyl-4-[2-(trifluoromethyl)phenyl]-, ethyl ester and 1.2 ml pyridine in 150 ml of dry ethanol-free CHCl3 at -10° C. The mixture was stirred for 45 minutes at 0° C. and the bromide (6 g) was obtained by flash chromatography over silica gel (10% EtAc/CH2Cl2). This was dissolved in 30 ml of THF and added dropwise to a suspension of 4-mercaptopyridine, sodium salt [(prepared from 1.5 g of 4-mercapto pyridine and 0.5 g of 60% NaH in THF/DMF (1:1, 40 ml)] at 0° C. and the mixture was warmed to room temperature. After stirring for one hour, the reaction mixture was diluted with water and extracted with CH2Cl2. The organic extracts were washed with water, dried, and evaporated. The residue was crystallized from EtAc to give 5.1 g of 3-pyridinecarboxylic acid, 5-cyano-1,4-dihydro-6-methyl-2[4-pyridinylthiomethyl]-4-[(2-trifluoromethyl)phenyl]-, ethyl ester, mp 222°-224° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723014
출처 데이터셋uspto-grants-1988_02
ORD IDord-d3c2e62310254be1a1f64db4e6e7ec04
출처 메모uspto-grants-1988_02