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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085335Generated: October 31, 2026

Methyl 2-(4-acetoxyphenoxy)propanoate → Propanoic acid, 2-(4-hydroxyphenoxy)-, methyl ester

https://huagongshe.com/reaction/1085335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(4-acetoxyphenoxy)propanoateHCID 20062087—
SolventMethanolHCID 887—
ProductPropanoic acid, 2-(4-hydroxyphenoxy)-, methyl esterHCID 36692698.3%

Reaction Steps

Methyl 2-(4-acetoxyphenoxy)propanoate (1.0 g, 4.2 mmol) is hydrolyzed by refluxing for 2 hours at 80° C. with methanol (10 mL) and concentrated HCL (36%, 2 drops). The reaction product is concentrated under reduced pressure to obtain methyl 2-(4-hydroxyphenoxy)propanoate (0.81 g). Conversion 99%, selectivity 99%, yield 97%; IR (neat) 1757 (vs) 1H NMR (CDC13) delta 1.60 (d, J=7.0 Hz, 3H), 3.80 (s, 3H), 4.85 (q, J=7.0 Hz, 1H), 6.82 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008439
Source datasetuspto-grants-1991_04
ORD IDord-b4dde146b87a4313943855c28d432f68
Source noteuspto-grants-1991_04