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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 386419생성일: 2026년 10월 26일

Ammonia hydroxide → Ethyl-[2-amino-3-nitro-6-(trifluoromethyl)-pyridin-4-yl]-benzylcarbamate

https://huagongshe.com/reaction/386419

반응식

참여 물질

역할이름HCID투입량
반응물Ammonia hydroxideHCID 21862953—
반응물Ethyl-[2-chloro-3-nitro-6-(trifluoromethyl)-pyridin-4-yl]-benzylcarbamateHCID 86614473—
용매TetrahydrofuranHCID 8028—
생성물Ethyl-[2-amino-3-nitro-6-(trifluoromethyl)-pyridin-4-yl]-benzylcarbamateHCID 67454545—

반응 조건

온도80 °C

반응 단계

Ethyl-[2-chloro-3-nitro-6-(trifluoromethyl)-pyridin-4-yl]-benzylcarbamate (63 gm 160 mmol) was dissolved in tetrahydrofuran (300 mL) and to this was added concentrated ammonia hydroxide solution (0.88 specific gravity, 100 mL) to give two phases. This was transferred to a pressure vessel, sealed and heated to 80° C. with stirring for 2 hours. The tetrahydrofuran was evaporated and the residue was partitioned between saturated brine and diethyl ether. The organic extracts were dried over sodium sulphate, filtered and evaporated to give a thick yellow slurry (65 gm) of ethyl-[2-amino-3-nitro-6-(trifluoromethyl)-pyridin-4-yl]-benzylcarbamate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372836B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-493de7e3cc1449e18b9110fb02cb4bee
출처 메모uspto-grants-2013_02