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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032242Generated: November 1, 2026

2,3-Dimethylquinoline → 8-(Bromomethyl)-7-chloro-3-methylquinoline

https://huagongshe.com/reaction/1032242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DimethylquinolineHCID 15591—
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
Reactant7-Chloro-3,8-dimethylquinolineHCID 13309788—
SolventWaterHCID 962—
Solvent1,2-DichlorobenzeneHCID 7239—
Product8-(Bromomethyl)-7-chloro-3-methylquinolineHCID 13309789—

Reaction Steps

9.6 g of 7-chloro-3,8-dimethylquinoline are dissolved in 850 g of 1,2-dichlorobenzene, 6.2 g of sodium acetate, dissolved in 150 ml of water, and then 8 g of bromine are added, and the mixture is exposed to a 150 watt low pressure mercury lamp for from 5 to 6 hours at 15° C. The yield, determined chromatographically, is 80% of theory, based on converted dimethylquinoline. The selectivity of the reaction is 88% at a conversion of 91%. Table 1 summarizes the result of varying the reaction conditions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957608
Source datasetuspto-grants-1990_09
ORD IDord-1a60238be49d4289ad042a251ca038c6
Source noteuspto-grants-1990_09