HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-Benzyloxyphenylacetyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Benzyloxyphenylacetic acid | HCID 81033 | — |
| Product | 4-Benzyloxyphenylacetyl Chloride | HCID 11357442 | — |
Reaction Steps
In this example, 6.05 g of 4-benzyloxyphenylacetic acid obtained as in Example 1, is dissolved in 125 ml of thionyl chloride, and boiled for 4 hours. Excess thionyl chloride is distilled off under reduced pressure, and the residue is dried, whereby 4-benzyloxyphenylacetic acid chloride is obtained. The thus obtained product is then dissolved in 25 ml of anhydrous benzene, and the resulting solution is added dropwise to 8.3 g of triethyl phosphite in a nitrogen gas stream with stirring under ice cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04733000 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-e70b1f8ae31b48ab8bd6366ff0d71c65 |
| Source note | uspto-grants-1988_03 |