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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106072Generated: October 30, 2026

1,3-Propanediol → 2-Chloromethyl-2-(2,5-dimethylphenyl)-[1,3]dioxane

https://huagongshe.com/reaction/2106072

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediolHCID 10442—
Reactant2-Chloro-1-(2,5-dimethylphenyl)ethan-1-oneHCID 2363693—
SolventO-XyleneHCID 7237—
Product2-Chloromethyl-2-(2,5-dimethylphenyl)-[1,3]dioxaneHCID 16050137—

Reaction Steps

A mixture of 18.3 g [0.1 mol] of 2-chloro-1-(2,5-dimethylphenyl)ethanone, 15.2 g [0.2 mol] of trimethylene glycol, 1.9 g [0.01 mol] of p-TsOH hydrate and 150 ml of xylene is heated to boiling with a water trap for about 5 hours. Part of the xylene is then distilled off, and the reaction mixture is extracted at room temperature with 30 ml of saturated aqueous NaCl solution and twice with 100 ml of water each time. The organic phase is dried over sodium sulfate and concentrated in vacuo, and all volatiles are distilled off up to about 87° C. under 0.25 mbar. 22.9 g of residue remain with, according to GC, 83.9% product (79.8% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579500B2
Source datasetuspto-grants-2009_08
ORD IDord-0b80a20ace484d69aa2ab34a6a9d32e7
Source noteuspto-grants-2009_08