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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719114Generated: November 1, 2026

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

https://huagongshe.com/reaction/719114

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, 2H, J=8.8 Hz), 6.88 (d, 2H, J=8.8 Hz), 5.03 (t, 1H, J=5.7 Hz), 4.40 (d, 2H, J=5.5 Hz), 4.05 (t, 2H, J=6.1 Hz), 3.77 (t, 2H, J=6.4 Hz); MS eI m/z 200.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132417B2
Source datasetuspto-grants-2006_11
ORD IDord-13fbd694139c490fadbb7506e959c982
Source noteuspto-grants-2006_11