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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204708Generated: November 2, 2026

Benzyl Bromide → HCID 66611362, compound

https://huagongshe.com/reaction/2204708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
ReactantHCID 66611811HCID 66611811—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66611362HCID 66611362—

Reaction Conditions

Temperature40 °C

Reaction Steps

Methyl 2-hydroxy-4-(1-piperidinylmethyl)-5-(trifluoromethyl)benzoate (may be prepared as described in Description 51; 230 mg, 0.72 mmol) was dissolved in N,N-dimethylformamide (5 mL) and cesium carbonate (264 mg, 0.81 mmol) and benzyl bromide (0.12 ml, 1.01 mmol) were added. The mixture was heated at 40° C. for 18 hours. Ethyl acetate (10 ml) and water (10 ml) were added and the organic layer was separated and washed with water (2×10 ml), dried (MgSO4) and the solvent removed in vacuo. Purification by column chromatography (1:1 cyclohexane/ethyl acetate-10% 7M NH3 in methanol/dichloromethane) gave the title compound as oil. 232 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365551B2
Source datasetuspto-grants-2016_06
ORD IDord-1eca90439bae4bdaa977fe65334a61f4
Source noteuspto-grants-2016_06