HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Ethoxycarbonylmethyl)triphenylphosphonium bromide → (5-Methylbenzofuran-2-yl)acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Ethoxycarbonylmethyl)triphenylphosphonium bromide | HCID 73731 | — |
| Reactant | 5-methyl-3H-benzofuran-2-one | HCID 10057646 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | (5-Methylbenzofuran-2-yl)acetic acid ethyl ester | HCID 70085569 | — |
Reaction Steps
A mixture of the product of Step 2, above (56) (10.81 mmol) and (carbethoxymethyl)triphenylphosphonium bromide (12.0 mmol) in 50 ml of xylene was heated to 155° C. for 20 hours. The reaction was cooled to ambient temperature and concentrated to dryness. The crude residue was chromatographed on silica gel with gradient elution with 5% EtOAc in hexanes to 10% EtOAc in hexanes to obtain the title compound (57).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789415 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-c08257b8fabf46059237a9ce479172fe |
| Source note | uspto-grants-1998_08 |