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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 637870생성일: 2026년 10월 26일

Thionyl Chloride → 2-Phenylbenzenesulfonyl isothiocyanate

https://huagongshe.com/reaction/637870

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물HCID 13422022HCID 13422022—
용매TolueneHCID 1140—
생성물2-Phenylbenzenesulfonyl isothiocyanateHCID 13422027—

반응 단계

77 g of potassium N-(2-biphenylylsulfonyl)carbonimidodithioate prepared in accordance with Example 2 was suspended in 100 ml of toluene, and 37 ml of thionyl chloride was added to the suspension at 0° to 10° C. over the course of 1 hour. After the addition, the mixture was stirred at room temperature for 2 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Distillation at reduced pressure gave 2-phenylbenzenesulfonyl isothiocyanate. On the other hand, 12.3 g of 2-amino-4,6-dimethylpyrimidine was suspended in 300 ml of dry toluene, and 27.5 g of 2-phenylbenzenesulfonyl isothiocyanate prepared as above was added. The mixture was heated under reduced pressure for 8 hours. After cooling, the resulting white precipitate was collected by filtration, and recrystallized from ethanol to give 31 g of the desired 1-(2-biphenylsulfonyl)3-(4,6-dimethylpyrimidin-2-yl)thiourea of the following formula, mp. 203°-204° C.: ##STR20##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04559079
출처 데이터셋uspto-grants-1985_12
ORD IDord-f7288056c5d74c808da8f35e1016e01b
출처 메모uspto-grants-1985_12