HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → HCID 11119343, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | HCID 11130420 | HCID 11130420 | — |
| Product | HCID 11119343 | HCID 11119343 | — |
Reaction Steps
The general procedure was used to convert phenylacetylene and (Z)-ethyl 3-iodo-3-phenylacrylate to the title product. Purification by flash chromatography (5% ethyl acetate in hexanes as the eluent) gave the analytically pure product as a light yellow oil (530 mg, 96% yield). 1H NMR (400 MHz, CDCl3) δ 7.78 (m, 2H), 7.63 (m, 2H), 7.38 (m, 6H), 6.59 (s, 1H), 2.06 (q, 2H), 1.35 (t, 3H). 13C NMR (100 MHz, CDCl3) δ 165.12, 136.92, 136.08, 131.85, 129.66, 128.99, 128.42, 128.18, 126.96, 122.54, 122.48, 101.88, 86.68, 60.16, 14.17. Anal. Calc'd. for C19H16O2: C, 82.58; H, 5.84; Found C,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473797B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-c71a3a3316004c0494cbfb120d3f1a79 |
| Source note | uspto-grants-2009_01 |