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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1758201생성일: 2026년 10월 26일

s-1,3-Benzothiazol-2-yl benzenecarbothioate → 2,2-Bis{4-[2-benzoyloxy-3-(7,7,9,9-tetramethyl-1,4-dioxa-8-azaspiro[4.5]dec-8-yl)propoxy]cyclohexyl}propane

https://huagongshe.com/reaction/1758201

반응식

참여 물질

역할이름HCID투입량
반응물s-1,3-Benzothiazol-2-yl benzenecarbothioateHCID 270394—
반응물2,2-Bis{4-[2-hydroxy-3-(7,7,9,9-tetramethyl-1,4-dioxa-8-azaspiro[4.5]dec-8-yl)propoxy]cyclohexyl}propaneHCID 20510600—
용매BenzeneHCID 241—
생성물2,2-Bis{4-[2-benzoyloxy-3-(7,7,9,9-tetramethyl-1,4-dioxa-8-azaspiro[4.5]dec-8-yl)propoxy]cyclohexyl}propaneHCID 20510562—

반응 단계

1.5 g of 2,2-bis{4-[2-hydroxy-3-(7,7,9,9-tetramethyl-1,4-dioxa-8-azaspiro[4.5]dec-8-yl)propoxy]cyclohexyl}propane and 1.2 g of 2-benzoylthiobenzthiazole were refluxed in 30 ml of anhydrous benzene for 4.5 hours. After completion of the reaction, the reaction mixture was treated with an aqueous alkali and then extracted with benzene, giving crystals. The crystals were purified by column chromatography through silica gel eluted with a 4:1 by volume mixture of diethyl ether and ethyl acetate. The desired Compound No. 222 was obtained in the form of a white powder melting at 77°-79° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04371644
출처 데이터셋uspto-grants-1983_02
ORD IDord-915f9cc3d87843bab679e9efbedb4fe3
출처 메모uspto-grants-1983_02