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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566509Generated: October 31, 2026

Benzyl Bromide → 1-[3-(Benzyloxy)-2-[(benzyloxy)methyl]-2-(4-bromobenzyl)propyl]-4-(diethoxymethyl)benzene

https://huagongshe.com/reaction/566509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-(4-Bromobenzyl)-2-[4-(diethoxymethyl)benzyl]-1,3-propanediolHCID 21265709—
SolventDimethylformamideHCID 6228—
Product1-[3-(Benzyloxy)-2-[(benzyloxy)methyl]-2-(4-bromobenzyl)propyl]-4-(diethoxymethyl)benzeneHCID 21265685—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2-(4-Bromobenzyl)-2-[4-(diethoxymethyl)benzyl]-1,3-propanediol(3 g, crude), benzyl bromide (3 mL), and NaH (1.2 g, 60% in mineral oil) in 30 mL of DMF was stirred for 14 h at 70° C. The mixture was then quenched with 5 mL of MeOH followed by 50 mL of saturated NH4Cl and extracted with 200 mL of 2:1 hexane/EtOAc. The extract was dried over Na2SO4 and concentrated. The residue was purified by silica gel chromatography eluted with 15:1 hexane EtOAc containing 1% of Et3N to give 2.5 g of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174874B1
Source datasetuspto-grants-2001_01
ORD IDord-1ee26cce31874b15b18e200ab3ca88e7
Source noteuspto-grants-2001_01