참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| 반응물 | (E)-3-(2,3-dihydrobenzo[b][1,4]dioxin-5-yl)acrylic acid | HCID 5343159 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Sodium Carbonate | HCID 10340 | — |
| 생성물 | (trans)-N-Methoxy-N-methyl-3-(2,3-Dihydrobenzodioxin-5-yl)propenamide | HCID 18787407 | — |
반응 단계
A mixture of (trans)-3-(2,3-dihydrobenzodioxin-5-yl)propenoic acid (9.83 g, 47.7 mmol), thionyl chloride (20 mL), and CH2Cl2 (75 mL) was heated to reflux for 1 hr, and then concentrated in vacuo to give a yellow-green solid. This material was dissolved in ethyl acetate (75 mL), and a solution of N,O-dimethylhydroxylamine hydrochloride (9.5 g) in saturated Na2CO3 (100 mL) was added with stirring. The mixture was stirred for 90 min and then diluted with water and ethyl acetate. The ethyl acetate layer was separated and washed twice with water and twice with saturated Na2CO3. The ethyl acetate layer was concentrated in vacuo to give a brown oil. This crude product was chromatographed on silica gel using 1:1 ethyl acetate/methylene chloride as the eluent to give a clear oil that crystallized upon standing (11.1 g, 93.1%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05981571 |
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| 출처 데이터셋 | uspto-grants-1999_11 |
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| ORD ID | ord-5d8267bb8b924f19a776bac7aeef0e02 |
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| 출처 메모 | uspto-grants-1999_11 |
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