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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637694Generated: October 30, 2026

1,5-Dibromopentane → HCID 20255654, compound

https://huagongshe.com/reaction/637694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DibromopentaneHCID 8100—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 20255642HCID 20255642—
SolventEthanolHCID 702—
ProductHCID 20255654HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04558043
Source datasetuspto-grants-1985_12
ORD IDord-1542bda883b74875abe7640ef616014e
Source noteuspto-grants-1985_12