HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2-Nitro-1-phenylbutan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1-Nitropropane | HCID 7903 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl aluminium dichloride | HCID 16686341 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Nitro-1-phenylbutan-1-ol | HCID 226123 | 29% |
Reaction Steps
To a solution of nitropropane (0.45 g, 0.005 moles) in dichloromethane (25 mL) at 0° C. was added triethylamine (0.67 mL, 0.005 moles) followed by ethyl aluminum dichloride (1.0 M in hexane, 5 mL, 0.005 moles). After 15 minutes benzaldehyde (0.5 mL 0.005 moles) was added and the solution allowed to warm to room temperature. After a further 3 hours the reaction was cooled in ice to a temperature of 5° C. and quenched with pH 7.0 phosphate buffer. The organic layer was separated, dried and evaporated in vacuo. Flash column chromatography [SiO2, 6:1 hexane, Et2O] gave 1-phenyl-2-nitro-1-butanol (0.28 g, 29%) Erythro:threo ratio 1:1.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04933505 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-d8a18e7ed19a42ab9a50f5bb802ded73 |
| Source note | uspto-grants-1990_06 |