참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylamine | HCID 674 | — |
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | 2-(2-Phenylethyl)malonic acid | HCID 101234 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-Methylene-4-phenylbutyric acid | HCID 13817411 | — |
반응 단계
A mixture of 2-phenylethylmalonic acid (1.8 g), 40% aqueous dimethylamine (1.08 ml, 1 eq) and 37% aqueous formaldehyde (0.64 ml, 1 eq) in water (10 ml) was stirred at room temperature overnight. After cooling at 0° C. the solid was filtered off, washed with water and dried. The white solid was heated at 170° C. for 10 minutes and cooled to room temperature. The resulting gum was dissolved in ethyl acetate (20 ml), washed with 10% potassium hydrogen sulphate solution (10 ml), water (2×10 ml), saturated brine (10 ml), dried (MgSO4) and evaporated to give crude 2-methylene4-phenylbutanoic acid. δH (CDCl3) 2.55-2.90 (4H, m, 2×CH,), 5.65, 6.85 (2H, 2×s, ##STR6## 7.25 (5H, m, Ph). The solid was dissolved in thioacetic acid (1 ml) and heated at 100° C. for 1 hour. After evaporation the gum was dissolved in ethyl acetate (10 ml) and extracted with saturated sodium hydrogen carbonate solution (2×10 ml). The combined extracts were washed with ethyl acetate (2×10 ml) and acidified with 10% potassium hydrogen sulphate solution (pH 3). The aqueous layer was extracted with ethyl acetate (2×10 ml) and the combined extracts washed with water (2×10 ml), dried (MgSO4) and evaporated to yield the title compound as a yellow oil (0.52 g, 24%); δH (CDCl3) 2.00 (2H, m, CH2), 2.71 (3H, m, CH2, CH), 3.14 (2H, m, CH2), 7.24 (5H, m, Ph). EIMS M+ 252 DCIMS MNH4+ 270.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06048852 |
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| 출처 데이터셋 | uspto-grants-2000_04 |
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| ORD ID | ord-af81b3554ce54b20925237650272ec7d |
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| 출처 메모 | uspto-grants-2000_04 |
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