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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39131Generated: October 26, 2026

1-(4-Methoxyphenyl)cyclopropane-1-carboxylic acid → Methyl 1-(4-methoxyphenyl)-cyclopropanecarboxylate

https://huagongshe.com/reaction/39131

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Methoxyphenyl)cyclopropane-1-carboxylic acidHCID 85575—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventMethanolHCID 887—
ProductMethyl 1-(4-methoxyphenyl)-cyclopropanecarboxylateHCID 137075441,980.2%

Reaction Steps

To a solution of 1-(4-methoxy-phenyl)-cyclopropanecarboxylic acid (50.0 g, 0.26 mol) in MeOH (500 mL) was added toluene-4-sulfonic acid monohydrate (2.5 g, 13.1 mmol) at room temperature. The reaction mixture was heated at reflux for 20 hours. MeOH was removed by evaporation under vacuum and EtOAc (200 mL) was added. The organic layer was washed with sat. aq. NaHCO3 (100 mL) and brine, dried over anhydrous Na2SO4 and evaporated under vacuum to give 1-(4-methoxy-phenyl)-cyclopropanecarboxylic acid methyl ester (53.5 g, 99%). 1H NMR (CDCl3, 400 MHz) δ 7.25-7.27 (m, 2H), 6.85 (d, J=8.8 Hz, 2H), H), 3.80 (s, 3H), 3.62 (s, 3H), 1.58 (q, J=3.6 Hz, 2H), 1.15 (q, J=3.6 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524767B2
Source datasetuspto-grants-2013_09
ORD IDord-e9933c517ae048b7ace1fe055d35c76f
Source noteuspto-grants-2013_09