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HRID 1090263作成日:2026年10月25日

Tetrahydrofuran → Ethyl 5-chloro-3-phenylthioindole-2-carboxylate

https://huagongshe.com/reaction/1090263

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物S-Phenyl benzenethiosulphonateHCID 71031—
反応物Ethyl 5-chloroindole-2-carboxylateHCID 78518—
反応物HCID 178418443HCID 178418443—
溶媒Diethyl EtherHCID 3283—
溶媒Ammonium ChlorideHCID 25517—
生成物Ethyl 5-chloro-3-phenylthioindole-2-carboxylateHCID 86745392—

反応手順

To a cold (0°), stirred solution of ethyl 5-chloroindole-2-carboxylate (223 mg) in 4.5 mL dry tetrahydrofuran, under argon, was added 0.55 mL of a solution of ethylmagnesium bromide in ether. The resultant mixture was stirred for 30 min then cooled to -78°. Solid S-phenyl benzenethiosulfonate (300 mg) was added and the mixture stirred at 78° for 30 min and 0° for 1 h. The mixture was then diluted with ether and saturated aqueous ammonium chloride added. The organic layer was separated, washed with water and brine and dried over MgSO4. Filtration and concentration gave a yellow oil which was purified by flash chromatography on silica gel. Elution with hexane-ethyl acetate (85:15) gave the title product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05081138
出典データセットuspto-grants-1992_01
ORD IDord-e0c79a883be944ecb464d0b26ed2382a
出典メモuspto-grants-1992_01