Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1967450생성일: 2026년 10월 27일
Hydrochloric Acid → ethyl 2-(5-bromo-2,4-dimethoxybenzoyl)-3-((S)-1-hydroxymethyl-2-methylpropylamino)acrylate
https://huagongshe.com/reaction/1967450
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | L-Valinol | HCID 640993 | — |
| 반응물 | Ethyl 2-(5-bromo-2,4-dimethoxybenzoyl)-3-dimethylaminoacrylate | HCID 66985486 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | ethyl 2-(5-bromo-2,4-dimethoxybenzoyl)-3-((S)-1-hydroxymethyl-2-methylpropylamino)acrylate | HCID 69031975 | — |
반응 단계
Under a nitrogen atmosphere, to a solution of ethyl 2-(5-bromo-2,4-dimethoxybenzoyl)-3-dimethylaminoacrylate obtained in Step 4 of Example 1 in toluene was added L-valinol (20.6 g). After stirring at room temperature for 1 hr, the completion of the reaction was confirmed by HPLC. 1 mol/L Hydrochloric acid (200 mL) was added to the reaction mixture, and after stirring, the toluene layer was separated. The toluene layer was further washed successively with 1 mol/L hydrochloric acid (200 mL), water (200 mL), 5% aqueous sodium hydrogencarbonate solution (200 mL) and water (200 mL). After washing, toluene was evaporated under reduced pressure, toluene (200 mL) was added to the concentrated residue, and the mixture was concentrated again under reduced pressure. THF (200 mL) was further added to the concentrated residue, and the mixture was concentrated again under reduced pressure. THF (160 mL) was added to the obtained concentrated residue to give ethyl 2-(5-bromo-2,4-dimethoxybenzoyl)-3-((S)-1-hydroxymethyl-2-methylpropylamino)acrylate as a tetrahydrofuran solution. The solution was directly used in the next step.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08420821B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-4030a6694aaf4968936276cd0de5717b |
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| 출처 메모 | uspto-grants-2013_04 |
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