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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657634Generated: November 1, 2026

Hydrochloric Acid → 1-(3-Acetamidophenoxy)-3-[2-(4-carbamoylphenoxy)ethylamino]propan-2-ol

https://huagongshe.com/reaction/1657634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
Reactant1-(3-Aminophenoxy)-3-[2-(4-carbamoylphenoxy)ethylamino]propan-2-olHCID 21535023—
SolventWaterHCID 962—
Product1-(3-Acetamidophenoxy)-3-[2-(4-carbamoylphenoxy)ethylamino]propan-2-olHCID 21535051—

Reaction Steps

An aqueous mixture consisting of 10 g. of 1-(3-aminophenoxy)-3-[2-(4-carbamoylphenoxy)ethylamino]propan-2-ol in 150 ml. of water was adjusted to pH 4-5 with dilute hydrochloric acid and then stirred vigorously for several minutes in order to effect complete solution. At this point, 3 g. of acetic anhydride were added to the mixture in a dropwise manner and the pH of the resulting solution was simultaneously maintained within the aforestated pH range by means of dilute aqueous sodium hydroxide. After further stirring the spent reaction mixture for a period of 1 hour, it was subsequently basified with additional dilute aqueous sodium hydroxide solution and the resulting solid precipitate with formed at this point was thereafter collected by means of suction filtration to give 1-(3-acetamidophenoxy)-3-[2-(4-carbamoylphenoxy)ethylamino]propan-2-ol as a white crystalline base, m.p. 164°-165°C. The analytical sample was then recrystallized from aqueous ethanol, but the melting point remained constant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03961072
Source datasetuspto-grants-1976_06
ORD IDord-e352066c7af949e2bf1b957c8a459e88
Source noteuspto-grants-1976_06