Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 53880984 | HCID 53880984 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54100099 | HCID 54100099 | — |
Reaction Steps
The aldehyde prepared in 2G (0.937 g, 3.77 mmoles) was dissolved in methanol (20 ml) and cooled to 0° C. Sodium borohydride (0.071 g, 1.87 mmoles) was added and the mixture was stirred 30 min. Acetone was added to react with an excess of sodium borohydride and then the reaction mixture was acidified with acetic acid. The solvents were evaporated under reduced pressure. The residue was diluted with ether and washed with water. The organic phase was dried over sodium sulfate, filtered and concentrated under reduced pressure to afford the title alcohol as an oil in a quantitative yield. NMR (H1, CDCl3, 60MHz) characteristic peaks 4 (t, JHH =7 Hz, 1), 5.1 (dt, JHF =21 Hz, JHH =8 Hz, 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05225429 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-15c95475b9ba45779a6a929d2a2d8b7e |
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| Source note | uspto-grants-1993_07 |
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