Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 626906생성일: 2026년 10월 26일
Hydrochloric Acid → Methyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylate
https://huagongshe.com/reaction/626906
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | p-tolylmethyl N-(pyrazine-2-carbonylamino)carbamate | HCID 478568 | — |
| 반응물 | 4-Methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carbonitrile | HCID 57468709 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Sodium Carbonate | HCID 10340 | — |
| 생성물 | Methyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylate | HCID 90015076 | 94% |
반응 단계
Concentrated aq. hydrochloric acid (42 mL, 491.4 mmol) was added to a stirred suspension of 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carbonitrile [CAS: 951232-17-0] (8.3 g, 31.53 mmol) in methanol (248 mL). The stirred mixture was heated at block temperature of 80° C. for 20 h. The reaction mixture was cooled to ambient temperature, diluted with DCM (500 ml) and Na2CO3 solid was added with stirring. Water (500 ml) was added and the mixture transferred to a separating funnel and shaken (aqueous phase had pH10). The aq. phase was re-extracted with DCM (200 ml) and the combined organic layers were dried (Na2SO4) and evaporated to an oil which solidified, to give 7.6 g after drying. This was dissolved in DCM (30 ml) and the solution was applied to a 340 g silica cartridge which was then eluted on a Biotage SP4 system with a gradient of EtOAc/iso-hexane from 0-75% to give methyl 4-methyl-6-[4-(trifluoromethyl)phenyl]pyrimidine-2-carboxylate (D29) (6.1 g, approximately 94% pure, contaminated with decarboxylated material);
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09309254B2 |
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| 출처 데이터셋 | uspto-grants-2016_04 |
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| ORD ID | ord-5af05b864aa940ceaa4065926d01a251 |
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| 출처 메모 | uspto-grants-2016_04 |
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