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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613329Generated: October 31, 2026

Hydrochloric Acid → N-[5-(4-Chlorophenyl)methyl-1,3-dioxan-2-yl]methylacetamide

https://huagongshe.com/reaction/1613329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-(4-Chlorobenzyl)propane-1,3-diolHCID 15096543—
ReactantN-(2,2-Dimethoxyethyl)acetamideHCID 15289457—
SolventDiethyl EtherHCID 3283—
ProductN-[5-(4-Chlorophenyl)methyl-1,3-dioxan-2-yl]methylacetamideHCID 1977574030%

Reaction Conditions

Temperature75 °C

Reaction Steps

4 g (20 mmol) of 2-[(4-chlorophenyl)methyl]propane-1,3-diol, 2.94 g (20 mmol) of N-(2,2-dimethoxyethyl)acetamide, 0.3 g of paratoluenesulphonic acid and 4 ml of diethyl ether saturated with hydrogen chloride are added to 150 ml of diethyl ether. The mixture is evaporated in vacuo, then 150 ml of benzene are added twice to the residue, it is heated to 70-80° C. under a slight vacuum and the solvent is evaporated. The residue is cooled, 150 ml of dichloromethane are added, and the solution is washed with a saturated solution of sodium hydrogen carbonate then with water and dried over magnesium sulphate. The residue is purified twice by chromatography on a silica gel column eluted with chloroform, and it is finally recrystallised in a 70:4 mixture of cyclohexane/ethyl acetate. 1.7 g (6 mmol) of product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192797
Source datasetuspto-grants-1993_03
ORD IDord-142aac11743945b08a226d4861578f0f
Source noteuspto-grants-1993_03