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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702510Generated: November 1, 2026

Hydrochloric Acid → HCID 12922708, compound

https://huagongshe.com/reaction/1702510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantBenzyl ChlorideHCID 7503—
Reactant3-Bromo-4-fluorobenzyl AlcoholHCID 2773351—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12922708HCID 1292270848.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

20.5 g (0.1 mol) of 3-bromo-4-fluoro-benzyl alcohol were added to a solution of 12.3 g (0.11 mol) of potassium tert.-butylate in 200 ml of tetrahydrofuran at 20° C. During this addition, the temperature increased to about 40° C. The mixture was subsequently stirred at 20° C. for about 1 hour and 12.6 g (0.1 mol) of benzyl chloride were then added dropwise to the reaction mixture. Thereafter, the mixture was heated under reflux for one hour. It was then cooled. About 200 ml of water and 50 ml of concentrated hydrochloric acid were added to the reaction mixture and the mixture was extracted twice with 200 ml of diethyl ether each time. The combined extracts were concentrated, dried over sodium sulphate and then subjected to fractional distillation. 14.2 g (48.2% of theory) of 3-bromo-4-fluoro-benzyl benzyl ether were obtained in the form of a light yellow oil of boiling point 165° C./7 mbars.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04381412
Source datasetuspto-grants-1983_04
ORD IDord-ab1c26cead4c449d97cfff3295ffd70d
Source noteuspto-grants-1983_04