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HRID 1929275作成日:2026年10月27日

Hydrochloric Acid → 3-fluoro-2-methylthio-4-trifluoromethylbenzoic Acid

https://huagongshe.com/reaction/1929275

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Dimethyl DisulfideHCID 12232—
反応物3-Fluoro-4-(trifluoromethyl)benzoic acidHCID 688293—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-fluoro-2-methylthio-4-trifluoromethylbenzoic AcidHCID 66864236—

反応手順

25.0 g (120.1 mmol) of 3-fluoro-4-trifluoromethylbenzoic acid were dissolved in 250 ml of dry tetrahydrofuran (THF), and 100.9 ml of n-butyllithium (2.5 M in hexane, 252.3 mmol) were added dropwise at −40° C. The mixture was stirred for 3 h, and a solution of 32.5 ml (360.4 mmol) of dimethyl disulfide in 50 ml of dry THF was then added dropwise. The mixture was stirred for 16 h, during which process, after half an hour, the temperature climbed slowly to RT. For work-up, 2 M HCl was added carefully. The mixture was extracted with diethyl ether, and the organic phase was subsequently extracted with 2 M NaOH. The aqueous phase was acidified and extracted with diethyl ether. The organic phase was washed with water, dried, and the solvent was removed in vacuo. The residue was stirred with n-heptane and the solid was separated off by a filtration. This gave 17.0 g of crude product, which was employed in the next synthesis step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08188009B2
出典データセットuspto-grants-2012_05
ORD IDord-bfdcaa7ae5c04f4aa34edae872076050
出典メモuspto-grants-2012_05