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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374834Generated: October 30, 2026

Hydroxyphenylacetic acid → HCID 13531056, compound

https://huagongshe.com/reaction/374834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyphenylacetic acidHCID 127—
Reactant1-PropanolHCID 1031—
ReactantThionyl ChlorideHCID 24386—
ProductHCID 13531056HCID 13531056—

Reaction Steps

A mixture of 4-hydroxyphenyl acetic acid (9.12 g, 0.06 mol), n-propanol (40 mL) and SOCl2 (2 mL, 0.028 mol) was refluxed for 3 hours, then evaporated in vacuo. The residue was extracted with ethyl acetate (200 mL), washed with 10% Na2CO3, then water dried (MgSO4), and evaporated in vacuo to give n-propyl 4-hydroxyphenylacetate as an oil. A solution of n-propyl 4-hydroxyphenylacetate (5.8 g, 0.03 mol) in epichlorohydrin (50 mL) was refluxed in the presence of DBU (2 mL, 0.014 mol for 2 hours. After the excess epichlorohydrin was removed, the residue was refluxed with isopropylamine (20 mL, 0.23 mol in n-propanol (50 mL), for 4 hours, then was evaporated in vacuo. The residue was crystallized from n-hexane to yield 3.8 g (41%) of n-propyl 4-(2-hydroxy-3-isopropylamino)propoxyphenylacetate, melting at 61°-62° C. and having the structural formula: ##STR29##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482961
Source datasetuspto-grants-1996_01
ORD IDord-46fd245b787b4e74a798ae140a53b13a
Source noteuspto-grants-1996_01