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HRID 2049342作成日:2026年10月26日

Carbon Disulfide → Cyanomethyl alpha-Methylbenzyl Trithiocarbonate

https://huagongshe.com/reaction/2049342

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DisulfideHCID 6348—
反応物ChloroacetonitrileHCID 7856—
反応物1-PhenylethanethiolHCID 141850—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物Cyanomethyl alpha-Methylbenzyl TrithiocarbonateHCID 2034506089%

反応条件

温度18 °C

反応手順

To a solution of 5.6 g (50 mmol) of potassium t-butoxide in 100 ml of tetrahydrofuran is added 8.7 ml (8.94 g, 60 mmol) of 92% 1-phenylethylmercaptan while maintaining the temperature of the reaction mixture between 20° and 25° C. The resulting suspension is cooled to 18° C. and 4.35 ml (72 mmol) of carbon disulfide is added thereto. The yellow solution which forms is stirred for 0.5 hours and then 3.23 ml (50 mmol) of chloroacetonitrile is added while the temperature of the reaction mixture is maintained at about 20° C. After stirring for 0.5 hour, the mixture is concentrated in vacuo. The residue is taken up in ether and the ether solution washed with water, brine, dried with Na2SO4 and concentrated in vacuo. The residue is chromatographed on a silica gel dry-column and eluted with 1:2 CH2Cl2 -hexane. The yellow band is collected to give 11.25 g (89%) of a yellow oil, cyanomethyl α-methylbenzyl trithiocarbonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04197311
出典データセットuspto-grants-1980_04
ORD IDord-d0d0f116bb3947b7aefd57f2f81d3661
出典メモuspto-grants-1980_04