HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → N-[4-(2-bromo-1-hydroxyethyl)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[4-(2-Bromoacetyl)Phenyl]Acetamide | HCID 12364739 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[4-(2-bromo-1-hydroxyethyl)phenyl]acetamide | HCID 22563212 | 18.9% |
Reaction Steps
To a solution of N-[4-(2-bromoacetyl)phenyl]acetamide (2.1 g, 0.0082 mol, in 30 mL of methanol) was introduced solid NaBH4 (1.0 g, 0.026 mol) at 0° C. and stirred at that temperature for 15 minutes. The mixture was diluted with diethyl ether (20 mL) and water (20 mL). The ether phase was separated and the aqueous phase was extracted with diethyl ether. The ether phases were combined and washed with brine, dried. Purification on a silica gel column gave the title compound as a white solid (0.40 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06852731B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-8ad6315898104647b2eb53bf2349ec6b |
| Source note | uspto-grants-2005_02 |