참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tributylamine | HCID 7622 | — |
| 반응물 | 2-Bromothiophene | HCID 13851 | — |
| 반응물 | Tri-o-tolylphosphine | HCID 80271 | — |
| 반응물 | N,N-Diisopropylacrylamide | HCID 559397 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N,N-Diisopropyl-3-(2-thienyl)propenamide | HCID 4444087 | — |
반응 단계
2-Bromothiophene (2.28 g, 14.0 mmol), N,N-diisopropylacrylamide (1.55 g, 10.0 mmol), palladium(II)acetate (34 mg, 0.15 mmol), tri-o-tolylphosphine (183 mg, 0.6 mmol), tri-n-butyl amine (2.04 g, 11.0 mmol) and dry DMF (5 mL) were mixed under a N2-atmosphere. The mixture was heated to 130° C. for 9 hours. Diethyl ether and H2O was added to the somewhat cooled mixture. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were washed twice with 2 M HCl, once with water, once with brine, and dried (MgSO4), and the solvent was then evaporated. The crude product was chromatographed on silica (petroleum ether-ethyl acetate 4:1), affording a yellow oil, 1.58 g (66%): 1H NMR (CDCl3) 67 1.35 (br, 12H), 3.9 (br, 1H), 4.1 (br 1H), 6.65 (d, 1H), 7.00-7.30 (m, 3H), 7.72 (d, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06313132B1 |
|---|
| 출처 데이터셋 | uspto-grants-2001_11 |
|---|
| ORD ID | ord-bd6dd6ada6b640f69bd0ffc231d41bb5 |
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| 출처 메모 | uspto-grants-2001_11 |
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