HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → 2-chloro-N-methyl-N-octylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Octylmethylamine | HCID 75538 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-chloro-N-methyl-N-octylacetamide | HCID 85690134 | 66.4% |
Reaction Steps
Chloroacetyl chloride in diethylether was added dropwise to N-methyloctylamine in diethylether at −2° C. The organic solution was returned to room temperature, followed by stirring for 3 hours. The resulting solution was successively washed with an aqueous 1 mol/L hydrochloric acid solution and water, and then dried over anhydrous sodium sulfate. After removal the solvent under vacuum, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=23:2) to give N-methyl-N-octyl-chloroacetamide (yield: 66.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609898B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-7fa9884aa2974055beceb669fdc98013 |
| Source note | uspto-grants-2013_12 |