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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293380Generated: October 26, 2026

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

https://huagongshe.com/reaction/1293380

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 numberUS07238724B2
Source datasetuspto-grants-2007_07
ORD IDord-1575e2ae4cb14f768dc353a4ebb4adcc
Source noteuspto-grants-2007_07