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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287450Generated: October 30, 2026

Ethyl bromoacetate → [1-Oxo-2-(2-chloroallyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid

https://huagongshe.com/reaction/1287450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Chloroallyl)-2-methyl-5-hydroxy-6,7-dichloro-1-indanoneHCID 20358457—
SolventDimethylformamideHCID 6228—
Product[1-Oxo-2-(2-chloroallyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acidHCID 20358440—

Reaction Steps

[1-Oxo-2-(2-chloroallyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid is prepared following substantially the same procedure described in Example 4, Step D, using the following reagents: 2-(2-chloroallyl)-2-methyl-5-hydroxy-6,7-dichloro-1-indanone (4.8 g., 0.0157 mole), potassium carbonate (6.0 g.), ethyl bromoacetate (4.5 ml.) and DMF (55 ml.). The above procedure gives 2.7 g. (48%) of [1-oxo-2-(2-chloroallyl)-2-methyl-6,7-dichloro-5-indanyloxy]acetic acid which after recrystallization from butyl chloride melts at 160°-162°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03984465
Source datasetuspto-grants-1976_10
ORD IDord-331836ae822047939a5f29a512066e86
Source noteuspto-grants-1976_10