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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835372Generated: October 30, 2026

Benzyl Bromide → HCID 23502804, compound

https://huagongshe.com/reaction/1835372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 178424180HCID 178424180—
CatalystHCID 178418647HCID 178418647—
SolventDichloromethaneHCID 6344—
ProductHCID 23502804HCID 2350280441%

Reaction Steps

A mixture of 50 mg (0.11 mmol) N-(3,5-bis-trifluoromethyl-benzyl)-6-hydroxy-N-methyl-4-o-tolyl-nicotinamide (Example 111), 0.014 ml (0.12 mmol) benzyl bromide and 59 mg (0.21 mmol) silver carbonate in 2 ml dichloromethane was heated at reflux for 2 h. Cooling to room temperature was followed by dilution with dichloromethane and filtration. The filtrate was washed with water. The aqueous layer was extracted with three portions of dichloromethane. The combined organic layers were dried with sodium sulfate, concentrated and dried in high vacuo. Column chromatography afforded 24 mg (41%) of the title compound as a viscous light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770637B2
Source datasetuspto-grants-2004_08
ORD IDord-70ac7d88daad423d87be8e226618d2ac
Source noteuspto-grants-2004_08