HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethoxyethane → 3-(7-Chloro-benzofuran-4-yl)-acrylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19611677 | HCID 19611677 | — |
| Reactant | Trimethylphosphonoacetate | HCID 53413272 | — |
| Product | 3-(7-Chloro-benzofuran-4-yl)-acrylic acid methyl ester | HCID 53784018 | — |
Reaction Steps
Trimethylphosphonoacetate (363 mg) in dry DME (1 ml) was added dropwise to a suspension of sodium hydride (60%; 329 mg) in dry DME (20 ml) at 0° under nitrogen. The resulting white precipitate was stirred for 40 mins at room temperature, then a solution of 7-chloro-benzofuran-4-carbaldehyde (intermediate 2) (1.238 g) in dry DME (15 ml) was added at room temperature over 1 min. The mixture was heated under reflux for 2 h, cooled to room temperature, then partitioned between water (150 ml) and ether (100 ml). The. combined organic extracts were washed with brine (100 ml) and dried (MgSO4). The solvent was evaporated to give the title compound as a colourless solid (1.59 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05981572 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-ded68973f0654c0cb1944dcf57465515 |
| Source note | uspto-grants-1999_11 |