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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2049342생성일: 2026년 10월 25일

Carbon Disulfide → Cyanomethyl alpha-Methylbenzyl Trithiocarbonate

https://huagongshe.com/reaction/2049342

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DisulfideHCID 6348—
반응물ChloroacetonitrileHCID 7856—
반응물1-PhenylethanethiolHCID 141850—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물Cyanomethyl alpha-Methylbenzyl TrithiocarbonateHCID 2034506089%

반응 조건

온도18 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04197311
출처 데이터셋uspto-grants-1980_04
ORD IDord-d0d0f116bb3947b7aefd57f2f81d3661
출처 메모uspto-grants-1980_04