HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitroethane → 1-(3-Bromophenyl)-3-nitrobutan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | (3-Bromophenyl)acetaldehyde | HCID 20387554 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Bromophenyl)-3-nitrobutan-2-ol | HCID 86711475 | 44% |
Reaction Steps
To a solution of 2-(3-bromophenyl)acetaldehyde (5.0 g, 0.025 mol) and DBU (7.6 mL, 0.05 mol) in THF (300 mL), Nitroethane (1.0 g, 0.03 mol) was added at 0° C. over 10 min. The reaction mixture was stirred for 3 h, quenched by the addition of H2O (50 mL) and extracted with EtOAc (100 mL×3). The combined organic layers were washed with H2O (2×30 mL) and brine (1×20 mL), dried over Na2SO4, filtered and concentrated to afford 1-(3-bromophenyl)-3-nitrobutan-2-ol (3.0 g, 44%) as a yellow oil. MS (ES+) C10H12BrNO3 requires: 273, 275 found: 274, 276 [M+2+H]+(1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115120B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-4f83e53b36d44ea9a677a8e887eb197a |
| Source note | uspto-grants-2015_08 |