HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromopentane → N-(4-(2-ethyl-1-hydroxybutyl)phenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromopentane | HCID 15738 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 4-Acetamidobenzaldehyde | HCID 73942 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-(2-ethyl-1-hydroxybutyl)phenyl)acetamide | HCID 22603035 | 52.2% |
Reaction Steps
A solution of 3-bromopentane (0.331 mol) in (C2H5)2O (200 ml) was added dropwise to a solution of magnesium turnings (0.331 mol) in (C2H5)2O, the mixture was stirred at RT for 2 hours and then cooled to 0° C. A solution of N-(4-formyl-phenyl)acetamide (0.11 mol) in THF (400 ml) was added dropwise and the mixture was stirred for 10 minutes. The mixture was poured into aqueous NH4Cl and extracted with EtOAc. The organic layer was dried, filtered off and the solvent evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97/3/0.1). The pure fractions were collected and evaporated, yielding 13.5 g (52%) of (±)-N-[4-(2-ethyl-1-hydroxybutyl)phenyl]acetamide (interm. 13).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07378433B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-2f3d43809ad24efcba765c426972a8cf |
| Source note | uspto-grants-2008_05 |