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HRID 3926作成日:2026年10月24日

Sodium hydride → Nicotinic Acid

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物SodiumHCID 5360545—
反応物tetrahydrofuran N,N-dimethylformamideHCID 21974620—
反応物pyridine-4-thiolHCID 178418431—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Nicotinic AcidHCID 938—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723014
出典データセットuspto-grants-1988_02
ORD IDord-d3c2e62310254be1a1f64db4e6e7ec04
出典メモuspto-grants-1988_02