Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86675339 | HCID 86675339 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19855884 | HCID 19855884 | — |
Reaction Steps
To a solution of 8-oxo-9-decenoic acid (910 mg, 4.94 mmol, 1.00 eq.) in MeOH (20.0 mL), was added CeCl3.7H2O (2.76 g, 7.41 mmol, 1.50 eq.). The mixture was stirred for 30 minutes with ice-cooling, and then thereto was slowly added sodium borohydride (224 mg, 5.93 mmol, 1.20 eq.). The mixture was stirred for 1 hour, and then the reaction solution was poured into 1 M aqueous hydrochloric acid solution. The organic phase was extracted with chloroform. Then, the resulting organic phase was dried over magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: chloroform/methanol=97:3) to obtain 8-hydroxy-9-decenoic acid as shown below (870 mg, 4.55 mmol, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073802B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-d0b388f9307c47cead958e456c66d9f1 |
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| Source note | uspto-grants-2015_07 |
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