참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 18-Crown-6 | HCID 28557 | — |
| 반응물 | 3-Thiophenecarboxaldehyde | HCID 68135 | — |
| 반응물 | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| 반응물 | Ethyl [bis(2,2,2-trifluoroethoxy)phosphinyl]acetate | HCID 11759356 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Thiophen-3-yl-acrylic acid ethyl ester | HCID 66914753 | 82.7% |
반응 단계
Potassium bis(trimethylsilyl)amide (3.92 g, 19.7 mol) was added to a solution of 18-Crown-6 (9.95 g, 37.6 mmol) and [Bis-(2,2,2 trifluoro-ethoxy)-phosphoryl]-acetic acid ethyl ester (6.54 g, 19.7 mmol) in dry THF (200 mL) at −78° C. After 30 minutes of stirring at this temperature, thiophene-3-carbaldehyde (2.0 g, 19.7 mmol) was added and the reaction was stirred for 3 hours at −780C after which the reaction was quenched with saturated ammonium chloride (200 mL). The reaction mixture was allowed to come to room temperature and was extracted with ethyl acetate (3×250 mL) and the combined organic extracts were washed with 10% HCl (200 mL), brine (200 mL) and dried with MgSO4 Evaporation of the solvent in vacuo gave the crude product that was purified by silica-gel chromatography using a 0-40% ethylacetate-hexane gradient to afford the subtitle compound (2.7 g, 82.7%). MS calculated for C9H10O2S+H: 183, observed: 183; 1H NMR (300 MHz, CDCl3, ppm) 1.31 (t, J=7 Hz, 3H); 4.22 (q, J=7 Hz, 2H); 5.83 (d, J=13 Hz, 1H); 6.87 (d, J=7 Hz, 1H); 7.24-7.28 (m, 1H); 7.54 (dd, J1=5 Hz, J2=1 Hz, 1H); 8.07 (br d, J=3 Hz, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423056B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-ac12fa240ab84c8694e525d002c85c2e |
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| 출처 메모 | uspto-grants-2008_09 |
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