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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540422Generated: October 30, 2026

Hydrochloric Acid → HCID 66988057, compound

https://huagongshe.com/reaction/540422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66988057HCID 66988057108%

Reaction Conditions

Temperature-70 °C

Reaction Steps

5 g (18.6 mmol) of ethyl N-(diphenylmethylene)glycinate in solution in 20 ml of tetrahydrofuran are added to a solution of 18.7 ml (18.6 mmol) of 1N potassium tert-butoxide in 20 ml of tetrahydrofuran cooled to −70° C. After stirring for 30 minutes, this mixture is added to a solution containing 3.2 g (18.6 mmol) of 4-methoxybenzoyl chloride in 20 ml of tetrahydrofuran at −70° C. One hour after the addition, the reaction medium is hydrolysed with a 1N aqueous solution of hydrochloric acid and concentrated. The residue is taken up in water and extracted with diethyl ether. The organic phase is dried over magnesium sulphate and the solvent is then evaporated off. 5.5 g of ethyl 2-amino-3-(4-methoxyphenyl)-3-oxopropanoate hydrochloride are obtained with a quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871187B2
Source datasetuspto-grants-2014_10
ORD IDord-1111e9371ee84d4faa6bd9d7a02fad31
Source noteuspto-grants-2014_10