HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloroacetyl chloride → Acetamide, 2,2-dichloro-N,N-bis(1-methylethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Acetamide, 2,2-dichloro-N,N-bis(1-methylethyl)- | HCID 79228 | — |
Reaction Steps
To a solution of diisopropylamine (6.8 g) (0.068 mol) and 6.8 g. of triethylamine in 100 ml of anhydrous benzene was added dropwise at 15° C. with stirring and ice-bath cooling, dichloroacetyl chloride (10.0 g, 0.068 mol). The solution was stirred overnight at room temperature. The benzene solution was washed successively with 10% HCl, H2O sodium hydroxide and saturated NaCl solution and was dried over anhydrous MgSO4. The solvent was distilled off, yielding 4.9 g. of liquid product, which infrared absorption spectra indicated to be substantially pure. No further purification was considered to be necessary for the purpose of this invention.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04208203 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-8bb65c6e7091410cb90035247171b927 |
| Source note | uspto-grants-1980_06 |