참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | 3-Methyl-2-butenoyl chloride | HCID 102394 | — |
| 반응물 | 4-Ethyl-4-hydroxymethyl-2-oxazolidinone | HCID 11263559 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 4-(3',3'-Dimethylacryloxymethyl)-4-ethyl-2-oxazolidinone | HCID 18413178 | — |
반응 단계
3.1 grains (0.021 mole) 4-ethyl-4-hydroxymethyl-2-oxazolidinone, prepared identically to that discussed in example 1, 2.6 grams (0.022 mole) 3,3-dimethylacryloyl chloride, and 25 milliliters chloroform were mixed in a one-necked round-bottom flask. The procedure employed was identical to that discussed in example 4. 410 grams (90% of the yield theoretically expected) of pure product was obtained as a yellow oil. The product exhibited the following spectral data: 1H NMR (CDCl3) δ0.98(t, 3H J=1.2 Hz), 1.65-1.71(m, 2H), 1.92(s, 3H), 2.17(s, 3H), 4.04-4.23(m, 4H), 5.71(s, 1H), 6.43(s, 1H); 13C NMR (CDCl3) δ7.6, 20.6, 27.7, 28.7, 60.3, 66.1, 71.3, 115.2, 159.0, 159.5, 166.2; IR (NaCl) 3215, 3020, 2970, 1785 cm-1 ; MS m/z 227. This monomer can be chlorinated or brominated by the same procedure as in example 1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05902818 |
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| 출처 데이터셋 | uspto-grants-1999_05 |
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| ORD ID | ord-51c6a024a99d4009a3ab8b21eb2e93eb |
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| 출처 메모 | uspto-grants-1999_05 |
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