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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11728Generated: October 25, 2026

Bromoacetonitrile → 4-(5-Chloro-2-hydroxy-phenyl)-4-oxo-butyronitrile

https://huagongshe.com/reaction/11728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetonitrileHCID 11534—
Reactant3-Chloro-6-hydroxyacetophenoneHCID 74061—
ReactantCarbonic acid, monomethyl ester, magnesium salt (2:1)HCID 167017—
SolventHydrochloric AcidHCID 313—
Product4-(5-Chloro-2-hydroxy-phenyl)-4-oxo-butyronitrileHCID 2197332258.6%

Reaction Steps

A solution of 1-(5-chloro-2-hydroxy-phenyl)-ethanone (1.0 g, 5.86 mmol) and magnesium methylcarbonate (13 mL, 32.5 mmol, 2.5 M solution in DMF) was stirred at 120° C. for 3 hours. The mixture was cooled to ambient temperature followed by the addition of bromoacetonitrile (1.22 mL, 17.6 mmol). The resulting solution was stirred at 90° C. for 3 hours. The reaction was cooled to ambient temperature then slowly poured into 1 M hydrochloric acid (200 mL). This was extracted with ethyl acetate, washed with brine, dried over magnesium sulfate, filtered and concentrated. Flash chromatography on silica gel gave the title compound (0.72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098212B2
Source datasetuspto-grants-2006_08
ORD IDord-17531f7d84eb482b9d2cd0545ab98c03
Source noteuspto-grants-2006_08