HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dibromobutane → 5-Chloro-3-methyl-6-(pyrrolidin-1-yl)-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Amino-5-chloro-3-methylbenzofuran | HCID 20255647 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Chloro-3-methyl-6-(pyrrolidin-1-yl)-benzofuran | HCID 20255649 | — |
Reaction Steps
A mixture of 9.1 g (50 mmole) of 6-amino-5-chloro-3-methylbenzofuran, 11.8 ml (0.1 mole) of 1,4-dibromobutane, 17.1 ml (0.1 mole) of N-ethyldiisopropylamine and 60 ml of ethanol is boiled under reflux for 24 hours and then concentrated by evaporation in vacuo. The residue is partitioned between methylene chloride and saturated sodium bicarbonate solution. The crude product obtained after drying and concentration by evaporation of the methylene chloride is chromatographed with petroleum ether/ether over silica gel. Subsequent distillation in a bulb tube (150°/10-1 torr) yields 5-chloro-3-methyl-6-(pyrrolidin-1-yl)-benzofuran having a melting point of 50°-52°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04558043 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-220f058344494205a4cde4decc2594ca |
| Source note | uspto-grants-1985_12 |