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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72976Generated: October 26, 2026

Methanol → 4-(3-Hydroxypropoxy)-3-methyl-benzoic acid

https://huagongshe.com/reaction/72976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-fluoro-4-(3-methoxyprop-1-ynyl)benzoateHCID 68153367—
Product4-(3-Hydroxypropoxy)-3-methyl-benzoic acidHCID 5513367785%

Reaction Steps

To methyl 3-fluoro-4-(3-methoxyprop-1-ynyl)benzoate (1.4 g, 6.3 mmol) in 2:1 mixture of THF: MeOH (15 mL) at room temperature was added 4 M sodium hydroxide solution (1.9 mL, 7.56 mmol) and reaction mixture was stirred for 1 hour. The solvent was removed in vacuo and the reaction mixture was extracted with ethyl ether, and layers were separated. The aqueous layer was acidified with 1M HCl solution and extracted with ethyl ether. The organics were separated, dried and concentrated in vacuo to give 4-(3-hydroxypropoxy)-3-methyl-benzoic acid (1.1 g, 85%) as a white solid. ESI-MS m/z calc. 208.2. Found 209.2 (M+1)+; Retention time: 1.22 minutes (3 min run); 1H NMR (400 MHz, CDCl3) δ 7.85 (dd, J=8.0, 1.4 Hz, 1H), 7.80 (dd, J=9.5, 1.3 Hz, 1H), 7.59-7.49 (m, 1H), 4.39 (s, 2H), 3.48 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828996B2
Source datasetuspto-grants-2014_09
ORD IDord-f706256cadfc4b6da62424f23cee4b08
Source noteuspto-grants-2014_09