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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072008Generated: October 29, 2026

Benzoyl chloride, 3,4-dichloro- → HCID 21409887, compound

https://huagongshe.com/reaction/2072008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3,4-dichloro-HCID 76403—
ReactantHCID 55284641HCID 55284641—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductHCID 21409887HCID 21409887—

Reaction Steps

A mixture of 2-allylmethylamino-2-methylpropylamine (1.3 g.,) and 3,4-dichlorobenzoyl chloride (3.15 g.,) was heated under reflux in dry benzene (150 ml.) for 1 hrs. The cooled mixture was washed with dilute sodium hydroxide solution (2 × 30 ml.), water (2 × 30 ml.), dried (MgSO4) and the solvent was removed in vacuo to give a yellow oil (3.9 g.). The oil was passed through a column of alumina 40 × 2.5 cm. using ethyl acetate as an eluent to give 3,4-dichloro-N-(2-allylmethylamino-2-methylpropyl)-benzamide as a pale yellow liquid (2.25 g., 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049663
Source datasetuspto-grants-1977_09
ORD IDord-f5fac60df1174815b1dc8098470d04b7
Source noteuspto-grants-1977_09