HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vinyl Chloride → 1,1-Dichloro-4-methyl-3-pentanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vinyl Chloride | HCID 6338 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1,1-Dichloro-4-methyl-3-pentanone | HCID 12656811 | — |
Reaction Steps
Anhydrous aluminium chloride (27.2 g) was added to a stirred solution of 2-methylpropionyl chloride (23.4 g) in dry trichloromethane (100 ml) with external cooling to between 0° C. and 15° C. Over a period of 1 hour chloroethene (20 g) was passed through the mixture held at 24°-26° C., after which stirring was continued for a further 40 minutes. The reaction mixture was then poured onto crushed ice, the organic layer was separated, dried over magnesium sulphate and distilled under reduced pressure to obtain a colourless liquid of 1,1-dichloro-4-methyl-3-pentanone. Yield 23 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753665 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-f38f30e8844e4ee8a1aa5ce3e33fc2c1 |
| Source note | uspto-grants-1998_05 |