HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 0-cyclopropylmethyl N-phenylacetyl-(2,6-dichlorophenyl)-acetamidoxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 0-Cyclopropylmethyl (2,6-dichlorophenyl)acetamidoxime | HCID 131725916 | — |
| Product | 0-cyclopropylmethyl N-phenylacetyl-(2,6-dichlorophenyl)-acetamidoxime | HCID 137242020 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
5.0 g (18 mmol) of 0-cyclopropylmethyl (2,6-dichlorophenyl)acetamidoxime in 40 ml of toluene were heated to 85° C and admixed with 3.9 g (25 mmol) of phenylacetyl chloride. The mixture was heated at 100° C. for 5 h, cooled, poured into aqueous sodium hydrogen carbonate solution (pH 7) and extracted three times with toluene. The combined extracts were washed with water, dried over sodium sulfate and concentrated under reduced pressure. The crude product (5.6 g) was purified by silica gel chromatography using cyclohexane/ethyl acetate. M.p. 134–135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101900B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-e65edce304774709b9289615e9c9e9ef |
| Source note | uspto-grants-2006_09 |