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HRID 1013974作成日:2026年10月27日

Hydrochloric Acid → 3-Chloro-5-(methylthio)benzonitrile

https://huagongshe.com/reaction/1013974

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DiisopropylethylamineHCID 81531—
反応物Sodium methanethiolateHCID 4378561—
反応物3-Bromo-5-chlorobenzonitrileHCID 15965893—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物3-Chloro-5-(methylthio)benzonitrileHCID 6687868676.6%

反応手順

(Step 1) A mixture of 3-bromo-5-chlorobenzonitrile (4.0 g), sodium methanethiolate (1.42 g), Pd2(dba)3 (84 mg), Xantphos (106 mg) and N,N-diisopropylethylamine (4.78 g) was stirred in toluene (100 ml) at 90° C. for 9 hr. The reaction mixture was treated with 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:20) to give 3-chloro-5-(methylsulfanyl)benzonitrile (2.6 g) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07982044B2
出典データセットuspto-grants-2011_07
ORD IDord-ea3122a97ef849578c019e71839db76c
出典メモuspto-grants-2011_07