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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597678Generated: November 1, 2026

Hydrochloric Acid → HCID 13305521, compound

https://huagongshe.com/reaction/597678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N-DimethylanilineHCID 949—
ReactantPhosgeneHCID 6371—
Reactant4-Methoxybenzyl alcoholHCID 7738—
ReactantDiethyl (hydroxyimino)malonateHCID 6399380—
ReactantDiethyl 2-chlorocarbonyloxyiminomalonateHCID 20567984—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 13305521HCID 13305521—

Reaction Steps

Benzene (20 ml.) was added to a solution of phosgene 2.5 g.) in benzene (11.4 ml.). A solution of diethyl 2-hydroxyiminomalonate (4.73 g.) and N,N-dimethylaniline (3.03 g.) in benzene (30 ml.) was added dropwise to the solution over 40 minutes at 5° C in a nitrogen stream. The mixture was stirred for 1 hour at the same temperature and overnight at room temperature. A solution of 4-methoxybenzylalcohol (3.11 g.) and pyridine (4.04 ml.) in benzene (30 ml.) was added dropwise to the resultant mixture containing diethyl 2-chlorocarbonyloxyiminomalonate over a period of 40 minutes at 5° C. The mixture was stirred for 2 hours at the same temperature, for 3 hours at room temperature and allowed to stand overnight. Cold water (100 ml.) was added to the reaction mixture to dissolve an insoluble material and cooled 1N-hydrochloric acid (20 ml.) was added thereto, after which the mixture was shaken. The organic layer was then washed 3 times with 1N hydrochloric acid (20 ml.), 3 times with a 5% sodium carbonate aqueous solution (20 ml.) and a sodium chloride aqueous solution, and then dried over magnesium sulfate. After drying, the solvent was distilled off to give diethyl 2-(4-methoxybenzyloxycarbonyloxyimino)malonate (6.89 g.), a pale brown oil, which was solidified on standing at ambient temperature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014915
Source datasetuspto-grants-1977_03
ORD IDord-f29a5c0bca0e407f9b570a3884a8d262
Source noteuspto-grants-1977_03