HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Vinylbenzoic acid → Ethyl 4-vinylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Vinylbenzoic acid | HCID 14098 | — |
| Reactant | Trimethylsilanylethyl 2-fluoro-4-iodobenzoate | HCID 54147505 | — |
| Product | Ethyl 4-vinylbenzoate | HCID 10866858 | — |
Reaction Steps
Employing the same general procedure as for the preparation of trimethylsilanylethyl 2-fluoro-4-iodobenzoate (Compound D), 323 mg (2.2 mmol) of 4-vinylbenzoic acid was converted into the title compound using 462 mg (2.4 mmol) of 1-(3-dimethylaminopropyl-3-ethyl carbodiimide hydrochloride), 264 mg (2.2 mmol) of 4-dimethylaminopyridine, 0.32 ml (250 mg, 5.45 mmol) of ethanol and 16 mL of dichloromethane. Purification by flash chromatography (silica, 10% ethyl acetate in hexane) gave the title compound as a clear, colorless oil. PMR (CDCl3): δ 1.39 (3 H, t, J=7.2 Hz), 4.37 (2 H, q, J=7.2 Hz), 5.38 (1 H, d, J=10.8 Hz), 5.86 (1 H, d, J=17.6 Hz), 6.75 (1 H, dd, J=10.8, 17.6 Hz), 7.46 (2 H, d, J=8.4 Hz), 8.00 (2 H, d, J=8.4 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06187950B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-5b746e6fb8ef4b50b3c134c5817cd6b9 |
| Source note | uspto-grants-2001_02 |