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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46293생성일: 2026년 10월 23일

tert-Butanol → tert-butyl N-(1,3-thiazol-4-yl)carbamate

https://huagongshe.com/ko/reaction/46293

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물TriethylamineHCID 8471—
반응물Diphenylphosphoryl azideHCID 123414—
반응물4-Thiazolecarboxylic acidHCID 304271—
생성물tert-butyl N-(1,3-thiazol-4-yl)carbamateHCID 5324163664.7%

반응 단계

Thiazole-4-carboxylic acid (6.46 g, 50.0 mmol) was slurried in tert-butyl alcohol (280 mL, 2900 mmol). Triethylamine (7.68 mL, 55.1 mmol) and diphenylphosphonic azide (11.9 mL, 55.1 mmol) were added and the reaction was heated at reflux for 18 hours. The reaction was evaporated to a residue. The residue was dissolved in ethyl acetate and washed with water, 5% citric acid (aqueous), water, saturated aqueous sodium bicarbonate and brine. The organic phase was dried over magnesium sulfate and evaporated to a residue. The residue was purified by silica gel chromatography (80 g ISCO™ column, hexanes to ethyl acetate gradient elution). Product fractions were combined and evaporated to a residue. The residue was triturated with 20% methyl t-butyl ether in hexanes. The solid was collected by filtration. Vacuum drying gave 6.48 g of product as a white solid. LCMS Rt=1.46 minutes MS m/z 201 [MH]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541588B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ca7487c3868f4ad7b197979b3124fb1e
출처 메모uspto-grants-2013_09