HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 12327003, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(4-Methoxynaphthalen-1-yl)-1-benzofuran | HCID 12326999 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12327003 | HCID 12327003 | — |
Reaction Steps
Alternatively, 3-methoxy-7-oxo-7H-benzo[b]-phenaleno[2,1-d]furan was prepared by addition of 0.38 ml. (45 mmol.) of oxalyl chloride followed by 1.2 ml. (0.01 mol.) of stannic chloride to a solution of 1 g. (37 mmol.) of 2-(4-methoxynaphthyl)benzofuran in 100 ml. of methylene chloride at 0°. The reaction mixture was stirred for 1.5 hours at 0° then poured into water. The layers were separated and the organic phase was washed with 10% aqueous sodium carbonate, dried (MgSO4) and evaporated to dryness. The residue was chromatographed on silica with chloroform as eluant to give the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985896 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-54bcbfa08a054062b4a9ce90bf79f2b9 |
| Source note | uspto-grants-1976_10 |