Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 90282105 | HCID 90282105 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90281956 | HCID 90281956 | 90.5% |
Reaction Steps
To a solution of 3-[4-(benzyloxy)-2-chlorophenyl]propanoic acid (1.00 g) in tetrahydrofuran (20.0 mL) was added 1,1′-carbonyldiimidazole (1.11 g), followed by stirring at room temperature for 2 hours. Subsequently, sodium borohydride (520 mg) and water (4.00 mL) were added thereto, followed by stirring at room temperature for 1 hour. To the reaction mixture was added 1 M hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 3-[4-(benzyloxy)-2-chlorophenyl]propan-1-ol (861 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199927B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-9958e59cb3c74789a497523c090c1feb |
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| Source note | uspto-grants-2015_12 |
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