Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 58442807 | HCID 58442807 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58442836 | HCID 58442836 | 177.7% |
Reaction Steps
A solution of 4-(3-methoxycarbonylfuran-2-yl)piperidine-1-carboxylic acid t-butyl ester (550 mg, 1.6 mmol, 1.0 eq.) in THF (15 mL) was added to a solution of LiAlH4 (120 mg, 3.2 mmol, 2.0 eq.) in THF (25 mL) at −30° C. The resulting solution was stirred for 1 hour and allowed to warm to 0° C., then stirred for 1 hour at 0° C. Water (120 mg) was added dropwise to quench the reaction. The mixture was allowed to warn to room temperature, and 15% NaOH (360 mg) and water (120 mg) was added. The mixture was stirred for 1 hour at room temperature. The solids were filtered and the filter cake was washed with EtOAc (20 mL). The residue was applied onto a silica gel column and purified by chromatography with PE/EtOAc (10:1˜5:1). The product was combined with another lot of material, then crystallized (PE/EtOAc=3:1, 1.2 mL), to yield 4-(3-hydroxymethylfuran-2-yl)piperidine-1-carboxylic acid t-butyl ester (0.8 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530663B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-420b6265862e4572b1196b12f0565b6e |
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| Source note | uspto-grants-2013_09 |
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