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HRID 39415作成日:2026年10月26日

Dimethyl Disulfide → 2-Methoxy-6-methylsulfanyl-4-trifluoromethyl-benzoic acid

https://huagongshe.com/reaction/39415

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl DisulfideHCID 12232—
反応物2-Methoxy-4-(trifluoromethyl)benzoic acidHCID 3690873—
反応物CID 53628100HCID 178418400—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methoxy-6-methylsulfanyl-4-trifluoromethyl-benzoic acidHCID 5919792111.1%

反応手順

N,N,N′N′-Tetramethylethylendiamine (21 g, 177 mmol) was added drop-wise at −70° C. to a solution of sec-butyllithium (110 mL, 1.4 M in cyclohexane, 154 mmol) in 180 mL tetrahydrofuran. 2-Methoxy-4-trifluoromethyl-benzoic acid (13 g, 59 mmol) in 60 mL tetrahydrofuran was added drop-wise at −70° C. over 2 hours. After complete addition stirring was continued at −70° C. for another 2 hours. Dimethyl disulfide (20 g, 207 mmol) was added at −70° C. within 10 min. Stirring was continued at −70° C. for another hour and the reaction was allowed to warm up. The reaction mixture was quenched with 150 mL water and extracted with 200 mL ethyl acetate. The aqueous phase was adjusted to pH1 by addition of 25% HCl and extracted twice with dichloromethane. The combined organic phases were dried on sodium sulfate, filtered and evaporated. The crude product was crystallized with heptane and yielded the title compound as a white solid (1.75 g, 11%), MS: m/e=265.1 [(M−H)−].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524909B2
出典データセットuspto-grants-2013_09
ORD IDord-cfeddf249152461fb69082a9f0fec78e
出典メモuspto-grants-2013_09