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HRID 1578205생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1578205

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 added dropwise 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.). The mixture was stirred for 30 minutes at the same temperature and allowed to stand overnight. A solution of tert-butyl alcohol (3.7 g.) and pyridine (4.0 g.) in benzene (50 ml.) was added dropwise for 20 minutes under ice-cooling to the resultant solution containing 1-chlorocarbonyloxy-6-chloro-1H-benzotriazole. 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 the resultant 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 desired compound (0.6 g.). Both quantities of crystals were mixed and dissolved in benzene. The resultant solution was then washed with a sodium bicarbonate aqueous solution and water and then dried. The solvent was removed by distillation to give the desired compound (3.2 g.), powder, mp 98° to 100° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE030752
출처 데이터셋uspto-grants-1981_09
ORD IDord-890b5ad0282741baa671d0f66590ead4
출처 메모uspto-grants-1981_09