HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobutyryl chloride → [4-(4-Chloro-1-oxobutyl)]-N-methoxy-N-methyl benzeneacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | N-Methoxy-N-methyl-2-phenylacetamide | HCID 10419762 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [4-(4-Chloro-1-oxobutyl)]-N-methoxy-N-methyl benzeneacetamide | HCID 9857023 | — |
Reaction Steps
Cool a slurry of aluminum chloride (87 g, 650 mmol) in methylene chloride (100 mL) with an ice bath. Add 4-chlorobutyryl chloride (51 g, 360 mL) dropwise over 0.5 hours. Add N-methoxy-N-methyl-benzeneacetamide (53 g, 300 mmol) over 0.5 hours. Allow the resultant solution to warm to room temperature. Then heat at reflux for 6 hours. Cool the solution to room temperature. Pour the solution into ice (1 L) and add methylene chloride (1 L). Separate the organic phase. Extract the aqueous phase with methylene chloride (2×500 mL). Dry the combined organics over anhydrous magnesium sulfate and concentrate to provide a solid which contains a ca. 1:1 mixture of the title compound and the meta isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06930197B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-cb63f374c42f44a4afc67627430e7141 |
| Source note | uspto-grants-2005_08 |