HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → HCID 67072655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | HCID 54757833 | HCID 54757833 | — |
| Product | HCID 67072655 | HCID 67072655 | — |
Reaction Steps
The title compound was prepared from ethynylbenzene (0.05 mL, 0.46 mmol) and trans-2-(4-iodophenyl)cyclopropanecarboxylic acid (100 mg, 0.35 mmol) according to the general procedure IC to give 47 mg (53%) of a white solid after purification by flash chromatography (SiO2, EtOAc:PE, 1:2→1:0): Rt=12.54 min (HPLC method I); 1H NMR (CDCl3) δ 7.53-7.51 (m, 2H), 7.47-7.44 (m, 2H), 7.36-7.31 (m, 3H), 7.09-7.07 (m, 2H), 2.63-2.58 (m, 1H), 1.95-1.90 (m, 1H), 1.72-1.67 (m, 1H), 1.44-1.39 (m, 1H); 13C NMR (CDCl3) δ 179.5, 140.0, 131.9, 131.7, 128.5, 128.4, 126.4, 123.4, 121.8, 89.7, 89.2, 27.1, 24.3, 17.8; ESI-MS calcd for C18H14O2 (M+Na+) 285.0887. found 285.0894.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586607B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-b7852b6a561d4922913269c09682f1de |
| Source note | uspto-grants-2013_11 |