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HRID 1405382作成日:2026年10月25日

Hydrochloric Acid → 4-(Isopropylthio)-3-methylbenzoic acid

https://huagongshe.com/reaction/1405382

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4-Bromo-3-methylbenzoic acidHCID 82131—
反応物Isopropyl propyl disulfideHCID 118529—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium HydroxideHCID 14798—
生成物4-(Isopropylthio)-3-methylbenzoic acidHCID 5855092634.5%

反応条件

温度-78 °C

反応手順

Butyllithium (16 mL of 1.6 M, 26 mmol) was added drop-wise to a mixture of 4-bromo-3-methyl-benzoic acid (2.5 g, 12 mmol) and THF (63 mL) at −78° C. The mixture was allowed to stir at −78° C. for 30 minutes before a solution of 2-isopropyldisulfanylpropane (1.7 g, 12 mmol) in THF (2 mL) was added drop-wise. The mixture was allowed to stir at −78° C. for 30 min, then 30 min at rt. The reaction mixture was then diluted with 100 mL of 1M aqueous sodium hydroxide. The organic layer was discarded and the aqueous layer was made acidic with 4M aqueous hydrochloric acid. The aqueous layer was then extracted 3 times with ethyl acetate. The combined extracts were dried over sodium sulfate and then evaporated to dryness. The crude material was purified by column chromatography using a gradient of 0-5% MeOH in dichloromethane to give 4-(isopropylthio)-3-methylbenzoic acid (870 mg, 18%). MS m/z calc. 210.3, found 211.2 (M+1)+. Retention time: 2.32 minutes (3 min run).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08916565B2
出典データセットuspto-grants-2014_12
ORD IDord-135aedca8eef4f78b9c2753b310dbc2c
出典メモuspto-grants-2014_12