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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618025Generated: October 26, 2026

Ammonium Chloride → 3-(4-Bromo-phenyl)-2-cyano-3-(2,4-difluoro-phenyl)-propionic acid ethyl ester

https://huagongshe.com/reaction/1618025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2,4-Difluoro-1-iodobenzeneHCID 137519—
ReactantEthyl 3-(4-bromophenyl)-2-cyanoprop-2-enoateHCID 367501—
ReactantHCID 178461733HCID 178461733—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Bromo-phenyl)-2-cyano-3-(2,4-difluoro-phenyl)-propionic acid ethyl esterHCID 66667330—

Reaction Steps

To a solution of 2,4-difluoro-1-iodo-benzene (12.0 g) in anhydrous THF (200 mL) was added a solution of isopropylmagnesium chloride lithium chloride complex (52.9 mL, 14% solution in THF) slowly over 10 min at room temperature. After stirring for 1 h, a solution of 3-(4-bromo-phenyl)-2-cyano-acrylic acid ethyl ester (10.0 g; example 74, step 1) in anhydrous THF (100 mL) was added and stirring continued at room temperature. After 1 h, a saturated aq. solution of ammonium chloride was added (100 mL), the phases separated and the aqueous layer extracted with ethyl acetate (3×100 mL). The combined organic phases were dried over sodium sulfate and the crude reaction product purified by silica gel chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane/ethyl acetate (1:0 to 3:1) to provide the title compound as a light yellow oil. MS (ESI−): m/z=391.9 ([M−H]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765730B2
Source datasetuspto-grants-2014_07
ORD IDord-2a1c076de48d4bdb84e293a8622722f7
Source noteuspto-grants-2014_07