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HRID 596216생성일: 2026년 10월 25일

Benzene → 1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazole

https://huagongshe.com/reaction/596216

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물PhosgeneHCID 6371—
반응물6-Chloro-1-hydroxy-1H-benzotriazoleHCID 232711—
반응물1-chlorocarbonyloxy-6-chloro-1H-benzotriazoleHCID 20567982—
용매PyridineHCID 1049—
용매tert-ButanolHCID 6386—
생성물1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazoleHCID 13292852—

반응 단계

A solution of phosgene (5 g.) in benzene (23.5 ml.) was dropwise added under ice-cooling to a suspension of 1-hydroxy-6-chloro-1H-benzotriazole (8.5 g.) and pyridine (3.9 g.) in benzene (50 ml.), and the mixture was stirred for 30 minutes at the same temperature and allowed to stand overnight. To the resultant solution containing 1-chlorocarbonyloxy-6-chloro-1H-benzotriazole was dropwise added, over 20 minutes under ice-cooling, a solution of tert-butyl alcohol (3.7 g.) and pyridine (4.0 g.) in benzene (50 ml.). The resultant mixture was stirred for 2 hours at the same temperature and allowed to stand overnight. The reaction mixture was filtered, and the filtrate was concentrated. Ether and petroleum ether were added to the residue to pulverize the residue and obtained crystals were collected by filtration to give 1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazole (5.3 g.). The mother liquor was concentrated to give the same object compound (0.6 g.). Both crystals were put together and dissolved in benzene, after which the solution was washed with a sodium bicarbonate aqueous solution and water and then dried. The solvent was removed by distillation to give the object compound (3.2 g.), powder, mp 98° to 100° C (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04010178
출처 데이터셋uspto-grants-1977_03
ORD IDord-1869df57661f4238a3d6a58ae4e3e5fe
출처 메모uspto-grants-1977_03