HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichlorobenzene → 2-(p-Methoxybenzoyl)-3-methyl-4-hydroxy-5-allylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | 2-(p-Methoxybenzoyl)-3-methyl-4-allyloxybenzofuran | HCID 15029668 | — |
| Product | 2-(p-Methoxybenzoyl)-3-methyl-4-hydroxy-5-allylbenzofuran | HCID 14579792 | 93% |
Reaction Steps
A solution of 2-(p-methoxybenzoyl)-3-methyl-4-allyloxybenzofuran (0.7 gm; 2.2 mmoles) in orthodichlorobenzene (3 mL) was refluxed under nitrogen for a period of 4 hours. The mixture was cooled to rom temperature and purified by chromatography on silica gel using 15% ethylacetate in hexane as eluent to yield 650 mg (93%) of 2-(p-methoxybenzoyl)-3-methyl-4-hydroxy-5-allylbenzofuran, mp. 48°-50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05087638 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-0b0e9bf7d21d48f389a4d7ca101fb811 |
| Source note | uspto-grants-1992_02 |