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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359039Generated: October 30, 2026

4-Fluorobenzyl bromide → Sodium 4-(4-fluorobenzyloxy)benzenesulfonate

https://huagongshe.com/reaction/1359039

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzyl bromideHCID 68021—
ReactantSodium P-phenolsulfonate dihydrateHCID 23666329—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
ProductSodium 4-(4-fluorobenzyloxy)benzenesulfonateHCID 2370136573.6%

Reaction Conditions

Temperature22 °C

Reaction Steps

To a stirred solution of 4-hydroxybenzenesulfonic acid sodium salt dihydrate (5.13 g, 22.1 mmol) in 23 mL of 1 N sodium hydroxide was added a solution of 4-fluorobenzyl bromide (3.3 mL, 26.5 mmol) in 20 mL of ethanol. The mixture was heated at reflux for two days, then cooled to ambient temperature (22° C.), whereupon a white precipitate formed. The flaky white solids were collected by filtration, rinsed with ethyl acetate and diethyl ether, and dried to give 4.95 g of 4-(4-fluoro-benzyloxy)-benzenesulfonic acid sodium salt. A stirred solution of 4-(4-fluoro-benzyloxy)-benzenesulfonic acid sodium salt (13.0 g, 42.7 mmol) in 50 mL of thionyl chloride and two drops of dimethylformamide was heated at a gentle reflux for 8 hours. The mixture was concentrated to a yellow solid which was suspended in ethyl acetate and filtered. The filtrate was concentrated to 11.2 g of 4-(4-fluorobenzyloxy)benzenesulfonyl chloride as a light yellow solid: 1H NMR (400 MHz, CDCl3) δ 7.95-7.98 (m, 2 H), 7.38-7.41 (m, 2 H), 7.06-7.12 (m, 4 H), 5.12 (s, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599890B1
Source datasetuspto-grants-2003_07
ORD IDord-4ca7c8f27a404cb5a805c7bd0b8709ce
Source noteuspto-grants-2003_07