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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520855Generated: November 4, 2026

Water → 4-(Cyclobutyl(hydroxy)methyl)benzoic acid

https://huagongshe.com/reaction/1520855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl 4-(cyclobutyl(hydroxy)methyl)benzoateHCID 68157714—
SolventMethanolHCID 887—
Product4-(Cyclobutyl(hydroxy)methyl)benzoic acidHCID 6815683577.2%

Reaction Steps

To a flask containing ethyl 4-(cyclobutyl(hydroxy)methyl)benzoate (530 mg, 2.26 mmol) was added tetrahydrofuran (5.60 mL), water (5.60 mL), and methanol (5.60 mL). Lithium hydroxide monohydrate (475 mg, 11.3 mmol) was then added. The suspension was stirred at room temperature for 18 hours. The reaction was quenched with 1 N hydrochloric acid to pH 3 and extracted three times with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated to give 490 mg of crude material. Purification by silica gel flash chromatography (0-20% ethyl acetate in heptane) afforded 4-(cyclobutyl(hydroxy)methyl)benzoic acid (360 mg, 77%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 8.07 (d, J=8.2 Hz, 2H), 7.43 (dd, J=8.0, 1.0 Hz, 2H), 4.67 (d, J=7.6 Hz, 1H), 2.62 (d, J=8.0 Hz, 1H), 2.09-1.98 (m, 2H), 1.91-1.80 (m, 4H). MS (M−1): 205.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073871B2
Source datasetuspto-grants-2015_07
ORD IDord-f96124c60dd44ea5a25d903a629241f5
Source noteuspto-grants-2015_07