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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289239Generated: October 30, 2026

Hydrochloric Acid → Methyl alpha-amino-p-methoxycarbonylmethylphenylacetate

https://huagongshe.com/reaction/1289239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl alpha-tert-butoxycarbonylamino-p-methoxycarbonylmethyl-phenylacetateHCID 54316225—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventDiethyl ether methanolHCID 21864698—
ProductMethyl alpha-amino-p-methoxycarbonylmethylphenylacetateHCID 54294376—

Reaction Steps

To a solution of methyl α-tert-butoxycarbonylamino-p-methoxycarbonylmethyl-phenylacetate (2.86 g, 8.5 mmol) in CH2Cl2 (10 ml) cooled at 0° C. was added 10 ml of TFA. After stirring for 1 hour at room temperature the reaction mixture was evaporated to dryness. The resulting solid was dissolved in ethyl acetate and water and the pH was adjusted to 8 with NaHCO3. After extraction with ethyl acetate the organic layers were washed with brine, dried and evaporated to give a yellow oil. After dissolution of this oil in a mixture of ether:methanol (10:1 v/v) a saturated solution of HCl in ether was added to give, after filtration, methyl α-amino-p-methoxycarbonyl-methylphenylacetate (2.2 g, 96%) as a white solid, m.p. 189.2°-189.6° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747499
Source datasetuspto-grants-1998_05
ORD IDord-9ec8b2b771ad4249893cd9784f39e532
Source noteuspto-grants-1998_05