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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855851Generated: October 26, 2026

Lithium hydroxide, monohydrate → 4-[(tert-Butyldimethylsilyl)oxy]cyclohexanecarboxylic Acid

https://huagongshe.com/reaction/855851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl 4-((tert-butyldimethylsilyl)oxy)cyclohexanecarboxylateHCID 23144129—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-[(tert-Butyldimethylsilyl)oxy]cyclohexanecarboxylic AcidHCID 5796071075.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of Example 45A (6.6 g, 23.0 mmol) in tetrahydrofuran (31 mL) and methanol (20 mL) was added lithium hydroxide monohydrate (1.93 g, 46.1 mmol). The resulting mixture was heated at 60° C. for 2 hours. The heat was removed and the reaction mixture was stirred at room temperature overnight. The solvents were removed in vacuo and the solution was neutralized with 1M HCl. Ethyl acetate (200 mL) was added and the layers were separated. The aqueous layer was further extracted with ethyl acetate (2×200 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated to give the titled compound (4.5 g). MS (CI) m/z 259 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262207B2
Source datasetuspto-grants-2007_08
ORD IDord-90de93dc0c684d838cdf2502b0cdcb71
Source noteuspto-grants-2007_08