HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22313292, compound → ethyl 2H-chromene-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22313292 | HCID 22313292 | — |
| Catalyst | Benzylidenebis(tricyclohexylphosphine)dichlororuthenium | HCID 11967259 | — |
| Product | ethyl 2H-chromene-6-carboxylate | HCID 22313317 | 82.7% |
Reaction Steps
To a stirred solution of ethyl 4-(allyloxy)-3-vinylbenzoate (1.8 g, 7.7 mmol) in CH2Ci2 (40 mL) at rt is added benzylidene-bis(tricyclohexylphosphine)dichlororuthenium (127 mg, 0.15 mmol). The mixture is stirred at rt for 2.5 h. The reaction mixture is concentrated in vacuo to a dark residue. The crude product is purified by flash chromatography on SiO2. Elution with hexanes-EtOAc (95:5) gives 1.3 g (80%) of ethyl 2H-chromene-6-carboxylate as a clear oil: 1H NMR (400 MHz, CDCl3) δ 7.8, 7.7, 6.8, 6.4, 5.8, 4.9, 4.4, 1.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06951868B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-a52c09c69253472baa09db874f907021 |
| Source note | uspto-grants-2005_10 |