Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638635Generated: October 26, 2026

Sodium hydride → 3-Bromo-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl ether

https://huagongshe.com/reaction/638635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-(4-Ethoxyphenyl)-2-methylpropanolHCID 158525—
Reactant3-Bromo-4-fluorobenzyl BromideHCID 12922710—
SolventDimethylformamideHCID 6228—
Product3-Bromo-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl etherHCID 1348819041.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

657 Milligrams of sodium hydride (as 60% oil suspension) was added to 10 ml of dimethylformamide, and 3.19 g of 2,2-dimethyl-2-(4-ethoxyphenyl)ethanol was added dropwise. Thereafter, the reaction solution was warmed to 50° C. and stirred for 10 minutes, and 4.0 g of 3-bromo-4-fluorobenzyl bromide was added dropwise thereto at 20° C. After completion of the dropwise addition, stirring was continued at 50° C. for further 5 hours, and the reaction solution was then poured into a 5% hydrochloric acid/ice water mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium chloride liquor and dried over anhydrous magnesium sulfate. After removing the solvent by evaporation, the residual oil was purified by column chromatography on a column packed with 60 g of silica gel to obtain 2.37 g of 3-bromo-4-fluorobenzyl 2,2-dimethyl-2-(4-ethoxyphenyl)ethyl ether. 1H-NMR spectrum (CDCl3, TMS). δ 7.4-6.5 (7H, m), δ 4.30 (2H, s), δ 3.99 (2H, q), δ 3.34 (2H, s), δ 1.36 (3H, t), δ 1.30 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562213
Source datasetuspto-grants-1985_12
ORD IDord-df932647de5b4769ac1dd2e1faf8da60
Source noteuspto-grants-1985_12