Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | HCID 10198312 | HCID 10198312 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | HCID 12494252 | HCID 12494252 | 93% |
Reaction Steps
Dissolve B-(2-(trimethylsilyl)ethynyl)-9-borabicyclo[3.3.1]nonane.tetrahydrofuran complex (2.13 g, 7.3 mmol) in pentane (25 mL) and add trimethylacetaldehyde (795 μL, 7.3 mmol). Stir at room temperature for 5 days. Remove the solvent under a positive nitrogen pressure to give a yellow solid. Add ethyl ether (30 mL) and methanol (500 μL). Cool to 0° C. and add, by dropwise addition, ethanolamine (440 μL, 7.3 mmol). Stir overnight, centrifuge the reaction mixture and separate the clear supernatant liquid. Wash the precipitate with pentane (2×10 mL) and combine the organic phases. Wash with water (2×25 mL) and dry (MgSO4). Evaporate the solvent in vacuo and purify by silica gel chromatography (19:1 hexane/ethyl acetate) to give the title compound as a clear liquid (1.25 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157167 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-d2408bb7c5294521a2931844d78cf054 |
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| Source note | uspto-grants-1992_10 |
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