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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80391Generated: October 27, 2026

Benzyl Bromide → Benzyl 4-(4-bromophenyl)-4-oxobutanoate

https://huagongshe.com/reaction/80391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Bromobenzoyl)propionic acidHCID 80646—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-(4-bromophenyl)-4-oxobutanoateHCID 5761095979%

Reaction Steps

Benzyl bromide (9.98 g, 58.3 mmol) was added to a solution of 4-(4-bromophenyl)-4-oxobutanoic acid (15.0 g, 58.3 mmol) and K2CO3 (3.5 g, 58.3 mmol) in DMF (300 mL) and stirred for 18 hours. The reaction mixture was partitioned between water (200 mL) and ethyl acetate (500 mL). Sat'd NaHCO3 soln (20 mL) was added and the aqueous layer extracted with ethyl acetate (2×) and the combined organic layers were washed with brine and dried and filtered. Concentration gave Example J5, benzyl 4-(4-bromophenyl)-4-oxobutanoate 16 g (79%) which was used without further purification. 1H NMR (500 MHz, CDCl3) δ 7.83 (d, J=8.6 Hz, 2H), 7.61 (d, J=8.5 Hz, 2H), 7.35-7.34 (m, 5H), 5.14 (s, 2H), 3.27 (t, J=6.7 Hz, 2H), 2.81 (t, J=6.7 Hz, 2H). HRMS: Anal. C17H16BrNO3 Calcd. 347.0277; found: 347.0283 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846023B2
Source datasetuspto-grants-2014_09
ORD IDord-84a5152c782b44fdb0429b093a9b0395
Source noteuspto-grants-2014_09