HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl cyanoacetate → HCID 11736980, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Benzene, 1-bromo-4-(trifluoromethyl)- | HCID 67872 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Product | HCID 11736980 | HCID 11736980 | 82% |
Reaction Steps
Method A of the above general procedure was followed using 4-bromobenzotrifluoride (226 mg, 1.01 mmol), ethyl cyanoacetate (123 mg, 1.09 mmol), pentaphenylferrocenyl ligand (14 mg, 0.020 mmol) and Pd(dba)2 (6.0 mg, 0.010 mmol). The reaction mixture was purified by column chromatography on silica gel (1:3 dichloromethane/hexanes) to give the desired product (213 mg, 82%) as a colorless oil: 1H NMR (CDCl3) δ 7.71-7.69 (m, 2H), 7.63-7.60 (m, 2H), 4.80 (s, 1H), 4.27 (dq, 7.2, 1.2 Hz, 2H), 1.30 (t, 7.2 Hz, 3H). 13C{1H} NMR (CDCl3) δ 164.28, 133.81, 131.66 (q, 33.0 Hz), 128.55, 126.38 (q, 3.7 Hz), 123.68 (q, 272.3 Hz), 115.00, 63.78, 43.52, 13.89.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562989B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-77dfe2e14a8d4ab49b269134094dfab9 |
| Source note | uspto-grants-2003_05 |