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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947715Generated: November 1, 2026

Benzyl Bromide → HCID 57907595, compound

https://huagongshe.com/reaction/1947715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 57907411HCID 57907411—
SolventDimethylformamideHCID 6228—
ProductHCID 57907595HCID 5790759568.4%

Reaction Steps

To a stirred solution of 60.0 g (236 mmol) of 4-[1-(tert-butoxycarbonyl)-1H-pyrazol-3-yl]butanoic acid from step C above in 400 mL of DMF was added 48.9 g (354 mmol) of potassium carbonate followed by dropwise addition of 40.0 mL (300 mmol) of benzyl bromide. The resulting mixture was stirred for 24 h, quenched with water, and extracted with ethyl acetate (3×300 mL). The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated to dryness in vacuo. The crude residue was purified by silica gel chromatography eluting with 30% ethyl acetate in hexanes to afford the title compound as a yellow oil (55.6 g. 68.4%). LC-MS: m/z (ES) 345 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399480B2
Source datasetuspto-grants-2013_03
ORD IDord-53a8adc969484821803d8f44ca07c11e
Source noteuspto-grants-2013_03