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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503626Generated: October 31, 2026

Ethyl bromoacetate → HCID 2899757, compound

https://huagongshe.com/reaction/1503626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantCesium carbonateHCID 10796—
Reactant3,5-Dichloro-4-hydroxybenzaldehydeHCID 16839—
SolventAcetoneHCID 180—
ProductHCID 2899757HCID 289975759.5%

Reaction Steps

To a solution of 3,5-dichloro-4-hydroxybenzaldehyde (302 mg, 1.6 mmol) in acetone (15 mL) was added cesium carbonate (700 mg, 2.15 mmol), followed by ethyl bromoacetate (0.27 mL, 2.43 mmol). The mixture was refluxed in acetone under stirring for 1 hour. After evaporation of acetone under reduced pressure, 100 ml, of water were added and the mixture was extracted with dichloromethane (200 mL). The organic phase was washed with brine (100 mL), dried over magnesium sulfate and concentrated under vacuum. The residue was purified by column chromatography over silica gel (eluent: dichloromethane) to give 264 mg of an oil (59% yield). 1H NMR (500 MHz, CDCl3): δ 1.29 (t, J=7.2 Hz, 3H), 4.26 (q, J=7.2 Hz, 2H), 4.85 (s, 2H), 7.96 (s, 2H), 9.98 (s, 1H). 13C NMR (126 MHz, CD3COCD3): δ 15.0, 62.3, 70.8, 131.2, 131.4, 135.4, 156.4, 168.4, 190.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212196B2
Source datasetuspto-grants-2015_12
ORD IDord-4d4bca612e604839a571fd18ca129007
Source noteuspto-grants-2015_12