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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ammonia hydroxide | HCID 21862953 | — |
| 반응물 | Ethyl-[2-chloro-3-nitro-6-(trifluoromethyl)-pyridin-4-yl]-benzylcarbamate | HCID 86614473 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethyl-[2-amino-3-nitro-6-(trifluoromethyl)-pyridin-4-yl]-benzylcarbamate | HCID 67454545 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08372836B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-493de7e3cc1449e18b9110fb02cb4bee |
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| 출처 메모 | uspto-grants-2013_02 |
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