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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235854Generated: November 2, 2026

Benzyl Bromide → 4-(Benzyloxy)-3-propylbenzonitrile

https://huagongshe.com/reaction/2235854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant4-hydroxy-3-propylBenzonitrileHCID 13987669—
CatalystWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(Benzyloxy)-3-propylbenzonitrileHCID 6701877382%

Reaction Steps

To a solution of 4-hydroxy-3-propylbenzonitrile (0.97 g, 6 mmol) (Example 29) in DMF (20 mL) were added 10 drops of water, benzyl bromide (2.05 g, 12 mmol), and Cs2CO3 (2.93 g, 9 mmol), and the mixture was stirred for 12 h at rt. The reaction mixture was concentrated under reduced pressure, and the residue was suspended in EtOAc and filtered. The precipitate was washed with more EtOAc. The combined filtrates were concentrated and purified by silica gel chromatography (EtOAc/hexanes (v/v)=1:19) to give 1.23 g (82%) of the title compound. 1H NMR (400 MHz, CDCl3): δ 7.48-7.32 (m, 7H), 6.92 (d, 1H), 5.13 (s, 2H), 2.67 (t, 2H), 1.72-1.60 (m, 2H), 0.98 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714004B2
Source datasetuspto-grants-2010_05
ORD IDord-d1dd8dbc4d694dd0b789906525c1a25f
Source noteuspto-grants-2010_05