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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308315Generated: November 1, 2026

4-Hydroxybenzyl Alcohol → 4-(3-Chloropropoxy)benzyl alcohol

https://huagongshe.com/reaction/2308315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantPotassium HydroxideHCID 14797—
ReactantPropane, bromochloro-HCID 36872—
SolventEthanolHCID 702—
Product4-(3-Chloropropoxy)benzyl alcoholHCID 22897496—

Reaction Steps

A solution of 4-hydroxy benzyl alcohol CAS No. [623-05-2] (10 g, 80.5 mmol) in ethanol (70 mL) was treated with 1, 3 bromochloro propane (16.0 g, 100 mmol) and potassium hydroxide (5.0 g, 89 mmol) was refluxed for 2 hours. The solution was cooled and filtered and then the filtrate concentrated. The concentrate was taken up in ether and washed with water, brine and dried over magnesium sulfate. The material was chromatographed on silica gel using ethyl acetate/hexanes (3:7) to yield 11.6 g of the product as a white solid: Mp=65° C.; 1H NMR (DMSO) 7.21 (d, 2 H, J=8.8 Hz), 6.88 (d, 2 H, J=8.8 Hz), 5.03 (t, 1 H, J=5.7 Hz), 4.40 (d, 2H, J=5.5 Hz), 4.05 (t, 2 H, J=6.1 Hz), 3.77 (t, 2 H, J=6.4 Hz); MS eI m/z 200.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06835729B2
Source datasetuspto-grants-2004_12
ORD IDord-de02a5237928404186b0c372bc4c6cc1
Source noteuspto-grants-2004_12