참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 4-Hydroxybutyl acrylate | HCID 75588 | — |
| 반응물 | 1-Chloroethyl chloroformate | HCID 521305 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-Chloroethyl 4-acryloyloxybutyl carbonate | HCID 53913051 | 90.2% |
반응 단계
Pyridine (0.89 ml, 11.00 mmol) is added dropwise to a solution of 1-chloroethyl chloroformate (1.20 ml, 11.00 mmol) and 4-hydroxybutyl acrylate (1.38 ml, 10.00 mmol) in dichloromethane (12 ml) at 3° C. under a dry N2 atmosphere. After 15 min. at 3° C. and 17 hours at 20° C. the reaction mixture is transferred to a separating funnel with the aid of dichloromethane (10 ml). The reaction mixture is washed with hydrochloric acid (1.00M, 10 ml), saturated aqueous sodium hydrogen carbonate (10 ml) and water (2×10 ml). The organic phase is dried (MgSO4) and the solvent evaporated under reduced pressure to give 2.26 g (90%) of the title product. 1H NMR (60 MHz, CDCl3): δ 1.80 (4 H, m, CH2 --CH2), 1.86 (3 H, d, J=5 Hz, CH3), 4.24 (4 H, m, 2×CH2 --O), 5.7-6.6 (4 H, m, CH=CH2 and CH).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05529766 |
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| 출처 데이터셋 | uspto-grants-1996_06 |
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| ORD ID | ord-1f317a034bee42acad9f18b0b29c762c |
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| 출처 메모 | uspto-grants-1996_06 |
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