HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-bromo-N-ethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzoyl chloride, 3-bromo- | HCID 74377 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-bromo-N-ethylbenzamide | HCID 4160271 | 95.2% |
Reaction Steps
To a solution of sodium hydroxide (3.80 g) in methanol (50 ml)—water (15 ml) was added by portions ethylamine hydrochloride (7.80 g) at 0° C. and the mixture was stirred for 5 min. 3-Bromobenzoyl chloride (5.53 g) was added dropwise and the mixture was stirrd at room temperature for 1 h. Methanol was evaporated under reduced pressure, and ethyl acetate was added to the residue for partitioning. The organic layer was washed with water and brine, dried (magnesium sulfate) and concentrated under reduced pressure. The residue was recrystallized from hexane-ethyl acetate to give the title compound (5.47 g) as colorless powder crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518257B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-d6a294882369475ca6cee65d6547307f |
| Source note | uspto-grants-2003_02 |