Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | 4-Chlorobutyronitrile | HCID 12336 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Product | 4-Octanone, 1-chloro- | HCID 10899007 | — |
Reaction Steps
A Grignard reagent is prepared from magnesium (1.9 g), n-butyl bromide (11.2 g) and dried ether (80 ml) and a solution of 4-chlorobutyronitrile (7 g) in ether (15 ml) is added dropwise to the reagent with ice-cooling. The mixture is stirred at the same temperature for 2 hours and then at room temperature for additional 2 hours. 10% Hydrochloric acid is slowly added dropwise to the mixture with ice-cooling to decompose the product and to acidify the mixture to pH about 1. After stirring at room temperature for 1 hour, the mixture is extracted with ether. The ether layer is washed with saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride and dried over magnesium sulfate. The solvent is distilled off and the residue is distilled to obtain 3-chloropropyl butyl ketone (1.6 g), b.p. 104°-106° C./30 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04372953 |
|---|
| Source dataset | uspto-grants-1983_02 |
|---|
| ORD ID | ord-c3b4eb3f8517430e8211a058c13ace5e |
|---|
| Source note | uspto-grants-1983_02 |
|---|