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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973336Generated: October 31, 2026

[2-(2-Amino-4-chlorophenoxy)phenyl]methanol → [2-(2-Acetamido-4-chlorophenoxy)phenyl]methyl acetate

https://huagongshe.com/reaction/1973336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[2-(2-Amino-4-chlorophenoxy)phenyl]methanolHCID 54153355—
SolventPyridineHCID 1049—
SolventAcetic AnhydrideHCID 7918—
Product[2-(2-Acetamido-4-chlorophenoxy)phenyl]methyl acetateHCID 20357201—

Reaction Steps

0.026 Part of 2-(2-amino-4-chlorophenoxy)benzyl alcohol is dissolved in 0.5 part pyridine and 0.5 part by volume acetic anhydride and allowed to stand at room temperature for 16 hours. The solvent is removed by evaporation under a nitrogen atmosphere and the resultant residue chromatographed on 0.6 part silicic acid. Elution with a 5:95 mixture of ethyl acetate-benzene and recrystallization from a mixture of ethyl acetate and benzene affords 2-(2-acetamido-4-chlorophenoxy)benzyl acetate. This compound melts at about 83° - 84° C. and is represented by the following structural formula. ##STR6## Elemental analysis shows C, 61.71%; H, 5.30%; Cl, 10.73%; N, 4.01%. The calculated values are C, 61.17%; H, 4.83%, Cl, 10.62%; and N, 4.20%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03997401
Source datasetuspto-grants-1976_12
ORD IDord-05ecc5afa10942f7bc4cff5f42b1befb
Source noteuspto-grants-1976_12