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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074549Generated: October 25, 2026

Water → Ethyl 2-(3-chloro-4-bromobenzyl)-1,2-dihydro-1-oxophthalazin-4-ylacetate

https://huagongshe.com/reaction/1074549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-(4-oxo-3,4-dihydrophthalazin-1-yl)acetateHCID 348622—
Reactant1-Bromo-4-(bromomethyl)-2-chlorobenzeneHCID 12947392—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(3-chloro-4-bromobenzyl)-1,2-dihydro-1-oxophthalazin-4-ylacetateHCID 2049580733.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 1,2-dihydro-1-oxophthalazin-4-ylacetate (11.5 g.) and sodium hydride (2.7 g.; 50% w/w dispersion in mineral oil) in dimethylformamide (125 ml.) was stirred at 60° C. for 1 hour under nitrogen. The solution obtained was cooled to room temperature and then 4-bromo-3-chlorobenzyl bromide (15.0 g.) was added, and the mixture stirred at 60° C. for 2 hours. After cooling to 25° C. the reaction mixture was poured into water (500 ml.). The aqueous mixture obtained was extracted with ethyl acetate (400 ml.). The extracts were washed with water, dried (MgSO4), and evaporated to give a solid, which was crystallised from propan-2-ol to yield ethyl 2-(3-chloro-4-bromobenzyl)-1,2-dihydro-1-oxophthalazin-4-ylacetate (7.3 g.), m.p. 142°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04393062
Source datasetuspto-grants-1983_07
ORD IDord-1bee9c7e61074308af24011cd4849793
Source noteuspto-grants-1983_07