HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-(2-Chloro-2-oxoethyl)phenyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [3-(Acetyloxy)phenyl]acetic acid | HCID 15029869 | — |
| Product | 3-(2-Chloro-2-oxoethyl)phenyl acetate | HCID 22480151 | — |
Reaction Steps
A solution of 6.36 g 3-acetoxyphenylacetic acid and 10 ml of thionyl chloride was refluxed for one hour. The solvent was removed on a rotary evaporator, 15 ml of dry benzene was added and re-evaporated to yield crude 3-acetoxyphenylacetyl chloride. To a cooled solution of the acid chloride in 35 ml benzene was added dropwise a solution 8.9 g of octyl amine and 10 ml of ether. The reaction mixture was stirred at room temperature for three hours, the solids filtered, and the filtrate transferred to a separatory funnel and extracted with 50 ml of 1 N HCl, 50 ml of H2O and 50 ml of brine. The resulting organic solution was dried (MgSO4), filtered, and evaporated to yield 10.14 g of a mixture containing octyl 3-acetoxyphenylacetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04424205 |
| Source dataset | uspto-grants-1984_01 |
| ORD ID | ord-f31f334e3aae4100a768332f5835a404 |
| Source note | uspto-grants-1984_01 |