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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462364Generated: October 31, 2026

Ammonia → HCID 53959586, compound

https://huagongshe.com/reaction/1462364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 54475721HCID 54475721—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53959586HCID 53959586—

Reaction Steps

20 ml of concentrated ammonia solution are added to a solution of 1.7 g of crude α-[N-[2-(3-carbomethoxy-4-hydroxy-phenoxy)-1-methyl-ethyl]-aminomethyl]-benzyl alcohol in 10 ml of dioxan and the mixture is left to stand at room temperature for 60-70 hours. The reaction mixture is evaporated, the residue is dissolved in 75 ml of ethyl acetate and the solution is washed with 10 ml of saturated, aqueous sodium chloride solution. Evaporation of the organic phase yields crude α-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-1-methyl-ethyl]aminomethyl]-benzyl alcohol as a mixture of diastereoisomers in the form of an oil and the latter is crystallised from a little ethyl acetate and is identical to the product obtained, for example, in Example 1; melting point 120°-140°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04460580
Source datasetuspto-grants-1984_07
ORD IDord-9c83767db7434cda88e71104bf60bf3a
Source noteuspto-grants-1984_07