HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,5-Dibromopentane → HCID 20255654, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 20255642 | HCID 20255642 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20255654 | HCID 20255654 | — |
Reaction Steps
A mixture of 8 g (49.6 mmole) of 6-amino-3,5-dimethylbenzofuran, 23 g (0.1 mole) of 1,5-dibromopentane, 12.9 g (0.1 mole) of N-ethyldiisopropylamine and 60 ml of ethanol is boiled under reflux for 18 hours. The residue obtained after concentration by evaporation in vacuo is taken up in methylene chloride and washed twice with dilute sodium bicarbonate solution. The organic phase is dried, concentrated by evaporation and the crude product is chromatographed with petroleum ether/methylene chloride over silica gel. Distillation of the pure fractions in a bulb tube (130°/10-1 torr) yields 3,5-dimethyl-6-piperidinobenzofuran having a melting point of 64°-66°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04558043 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-1542bda883b74875abe7640ef616014e |
| Source note | uspto-grants-1985_12 |