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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl [4-(azidoacetyl)phenoxy]acetate | HCID 5155020 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(aminoacetyl)phenoxyacetate hydrochloride | HCID 20315552 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04105790 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-3604bc81c75d4d32b3530adfc8532c45 |
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| Source note | uspto-grants-1978_08 |
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