HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863172Generated: October 30, 2026
Sodium borohydride → HCID 57050928, compound
https://huagongshe.com/reaction/863172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 57102460 | HCID 57102460 | — |
| Reactant | HCID 178526981 | HCID 178526981 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57050928 | HCID 57050928 | 83% |
Reaction Steps
To a mixture of methyl (1S,6R)-3,3-dimethyl-6-(1-methylvinyl)-2-oxocyclohexane-1-carboxylate (1.38 g) and cerium (II) chloride heptahydrate (2.14 g) in methanol (10 ml) was added sodium borohydride (217 mg) at 0° C. The mixture was stirred at room temperature for 1 hr, and the reaction was quenched by addition of water. The pH of the mixture was adjusted to pH 7 with 0.1N hydrochloric acid. The mixture was extracted with ether. The combined organic extracts were washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated. Purification of the residue by flash column chromatography (using n-hexane:ethyl acetate=20:1 as an eluent) gave methyl (1S,2R,6R)-2-hydroxy-3,3-dimethyl-6-(1-methylvinyl)cyclohexane-1-carboxylate (1.15 g, 83% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05719291 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-4c1684f3a0c64436a4a372b34a6e16d3 |
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| Source note | uspto-grants-1998_02 |
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