HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 67996287, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67427596 | HCID 67427596 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67996287 | HCID 67996287 | — |
Reaction Steps
A 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer was charged with 27 (800 mg, 1.86 mmol) and ethanol (5.0 mL). Sodium borohydride (69 mg, 11.82 mmol) was added in one portion. The mixture was stirred at room temperature for 1 h and then neutralized with acetic acid to pH 7. The reaction was concentrated under reduced pressure and triturated with ethyl acetate (10 mL) to give a quantitative yield of 28 as a white semi-solid: 1H NMR (500 MHz, CDCl3) δ 8.75 (d, 1H, J=8.5 Hz), 7.78 (s, 1H). 7.53 (m, 2H), 7.10 (m, 1H), 4.58 (s, 1H), 2.88 (d, 1H, J=16.0 Hz), 2.69 (d, 1H, J=16.0 Hz), 1.32 (s, 12H), 1.20 (d, 611, J=6.5 Hz); MS (APCI+) m/z 431.4 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598174B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-e5750cdab7e34561819420f17a600d12 |
| Source note | uspto-grants-2013_12 |