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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371291Generated: October 30, 2026

Benzyl Bromide → HCID 67486384, compound

https://huagongshe.com/reaction/2371291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
ReactantBenzeneacetic acid, 4-(1,1-dimethylethyl)-HCID 118343—
SolventDimethylformamideHCID 6228—
ProductHCID 67486384HCID 67486384—

Reaction Steps

To a stirred solution of 4-tert-butyl-phenyl acetic acid (5.0 g, 26.04 mmol) in DMF (30 mL) at rt were added Cs2CO3 (12.72 g, 39.06 mmol) and benzyl bromide (4.89 g, 28.6 mmol). The reaction mixture was stirred for overnight at room temperature and then the reaction mixture was heated at 100° C. for 1 h and cool to rt. The solvent was removed under reduced pressure and poured into cold 1 N HCl (50 mL). The aqueous solution was extracted with ethyl acetate (2×100 mL) and the combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure, dried under vacuum. (4-tert-butyl-phenyl)acetic acid benzyl ester was obtained as a yellowish liquid. (5.96 g, 81%): 1H NMR (300 MHz, CDCl3): δ 7.37-7.33 (m, 7H), 7.25 (dd, J=5.4, 13.2 Hz, 2H), 5.14 (s, 2H), 3.65 (s, 2H), 1.32 (s, 9H); TLC conditions: Uniplate silica gel, 250 microns; mobile phase=ethyl acetate-hexanes (1:5); Rf=0.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710236B2
Source datasetuspto-grants-2014_04
ORD IDord-f87eb71bf0bc49d184018fa1e6a2509a
Source noteuspto-grants-2014_04