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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419381Generated: November 1, 2026

Hydrochloric Acid → Methyl 4-(aminoacetyl)phenoxyacetate hydrochloride

https://huagongshe.com/reaction/2419381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl [4-(azidoacetyl)phenoxy]acetateHCID 5155020—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(aminoacetyl)phenoxyacetate hydrochlorideHCID 20315552—

Reaction Conditions

Temperature40 °C

Reaction Steps

Methyl 4-(azidoacetyl)phenoxyacetate (2.49g.) was added to a stirred solution of triphenylphosphine (2.62g.) in tetrahydrofuran (20ml.) maintained at 40° C. The solution gradually became orange during the addition of the azido compound and was further stirred at 40° C. for 15 minutes after the addition was complete. 1N-Hydrochloric acid (20ml.) was then added and the mixture stirred at 40° C. for 15 minutes. The mixture was cooled to room temperature and then ether (200ml.) was added. The ethereal layer was decanted off and the brown oily residue was dissolved in toluene (20ml.) and the solution obtained was evaporated in vacuo. The solid residue formed was then recrystallised twice from methanol to give methyl 4-(aminoacetyl)phenoxyacetate hydrochloride (0.7g.), m.p. 202°-204° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105790
Source datasetuspto-grants-1978_08
ORD IDord-3604bc81c75d4d32b3530adfc8532c45
Source noteuspto-grants-1978_08