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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035413Generated: October 29, 2026

2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- → Ethyl 1-benzylazetidine-3-carboxylate

https://huagongshe.com/reaction/2035413

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ReactantDiethyl 1-benzylazetidine-3,3-dicarboxylateHCID 11483175—
CatalystTetraethylammonium acetate tetrahydrateHCID 2724098—
SolventWaterHCID 962—
ProductEthyl 1-benzylazetidine-3-carboxylateHCID 53429348—

Reaction Conditions

Temperature130 °C

Reaction Steps

Tetraethylammonium acetate tetrahydrate (9.42 g) was added to a 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU, 40 mL) solution of diethyl 1-benzylazetidine-3,3-dicarboxylate (7.00 g, which was prepared according to the method described in Synthetic Communications, volume 33, No. 19, page 3347, 2003), followed by stirring at 130° C. for 12 hours. The reaction solution was added with water, and extracted with an ethyl acetate-hexane (1:1) mixed solvent. The organic layer was washed with water, hexane was added, and extracted with 0.5 mol/L hydrochloric acid. The aqueous layer was washed with tert-butyl methyl ether, and the pH was adjusted to 8 using a 5 mol/L aqueous sodium hydroxide solution, followed by further extraction with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated, to thereby obtain the title compound (3.21 g) having the following physical properties.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575134B2
Source datasetuspto-grants-2013_11
ORD IDord-0fd94681ff0841beace775b4276afad8
Source noteuspto-grants-2013_11