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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363298Generated: November 1, 2026

Benzyl Bromide → HCID 53922389, compound

https://huagongshe.com/reaction/363298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantWater ethylacetateHCID 22728543—
ReactantHCID 53745759HCID 53745759—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDimethylformamideHCID 6228—
ProductHCID 53922389HCID 53922389105.3%

Reaction Steps

A mixture of the title compound of Step D (0.5 g, 2.46 mmol), K2CO3 (1.02 g, 7.38 mmol), benzyl bromide (0.463 g, 2.71 mmol) and TBAB (79 mg) in DMF (5 mL) was stirred at room temperature for 48 h. After the reaction was complete, the reaction mixture was poured into an H2O/ethyl acetate mixture (10/100 mL). The organic phase was separated, dried and concentrated to give the title compound of Step E as a brown solid (0.76 g). 1H NMR (CDCl3, 300 MHz): δ 7.32 (m,6H, aromatic) 6.72 (d,1H, 11 Hz), 6.34 (d,1H, 8 Hz), 4.82 (s,2H), 4.69 (s,2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874382
Source datasetuspto-grants-1999_02
ORD IDord-62bc8b92bd3240c8823d46bcd7e5f226
Source noteuspto-grants-1999_02