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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Ethyl 4-((tert-butyldimethylsilyl)oxy)cyclohexanecarboxylate | HCID 23144129 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[(tert-Butyldimethylsilyl)oxy]cyclohexanecarboxylic Acid | HCID 57960710 | 75.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07238724B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-1575e2ae4cb14f768dc353a4ebb4adcc |
|---|
| Source note | uspto-grants-2007_07 |
|---|