HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525499Generated: October 30, 2026
Lithium tri-s-butylborohydride → HCID 178504290, compound
https://huagongshe.com/reaction/525499
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium tri-s-butylborohydride | HCID 3611392 | — |
| Reactant | HCID 4060849 | HCID 4060849 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178504290 | HCID 178504290 | 52.7% |
Reaction Steps
To a solution of L-selectride (165 mL, 0.165 mol, 1.5 eq) in anhydrous THF (200 mL) at −78° C. was added dropwise a solution of 4-(trimethylsilyl)cyclohexanone (20 g, 0.11 mol, 1.0 eq) in anhydrous THF (100 mL). The temperature was maintained for 3 h, and then the reaction mixture was stirred at room temperature for 16 h. Then the mixture was cooled to 0° C. before being quenched with water. The resulting mixture was warmed up to room temperature, and then sodium hydroxide aqueous solution (80 mL, 3 M) was added, followed by hydrogen peroxide (80 mL, 30%). After being stirred for 3 h, the mixture was extracted with EtOAc (300 mL×3), and the combined organic layers were washed with H2O and brine, dried over Na2SO4, concentrated to give a residue which was purified by column chromatography on silica gel (petroleum ether/EtOAc=10:1) to obtain the product cis-4-(trimethylsilyl)cyclohexanol as a white solid (10.0 g, 51% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340527B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-9abe24bea90d4cf9a4fd990109302e1e |
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| Source note | uspto-grants-2016_05 |
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