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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771713Generated: October 30, 2026

HCID 81430592, compound → Methyl 3-bromo-5-cyanobenzoate

https://huagongshe.com/reaction/1771713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 81430592HCID 81430592—
SolventPhosphorus oxychlorideHCID 24813—
ProductMethyl 3-bromo-5-cyanobenzoateHCID 2194261596.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To methyl 3-bromo-5-carbamoyl-benzoate (2.8 g, 10.8 mmol, 1.0 eq) was added POCl3 (30 mL) and the reaction heated at 100° C. overnight. The POCl3 was removed under reduced pressure, water was added and the aqueous layer extracted with EtOAc. The combined organic extracts were dried (Na2SO4), filtered and evaporated in vacuo to afford a crude residue which was purified by column chromatography (petroleum ether:EtOAc, 20:1) to give methyl 3-bromo-5-cyano-benzoate (2.5 g, 96%). This material was dissolved in THF (30 mL) and LiOH.H2O (1.7 g, 41.6 mmol, 1.54 eq) and H2O (10 mL) were added. The mixture was stirred at room temperature overnight. The THF was removed under reduced pressure and the aqueous phase acidified with diluted HCl and extracted with EtOAc. The combined organic extracts were dried (Na2SO4), filtered and evaporated in vacuo. The residue obtained was purified by column chromatography (CH2Cl2: MeOH, 50:1) to give the title compound as a white solid (2 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249085B2
Source datasetuspto-grants-2016_02
ORD IDord-3546e09a696f409ba2535a6c729bdbe7
Source noteuspto-grants-2016_02