HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → HCID 17956193, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | HCID 17956195 | HCID 17956195 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 17956193 | HCID 17956193 | — |
Reaction Steps
A solution of the product from Example 4(i) (1 g, 2.8 mmol) in dry DCM was stirred at 0° C. under nitrogen. Anisoyl chloride (4.9 mmol) was added followed by a solution of SnCl4 (1M DCM, 4.9 mmol). An immediate red colour occurred and stirring was continued for 2 hours. The reaction mixture was added carefully to 100 ml of ice-water and the aqueous was extracted with ethylacetate (3×100 Ml). The organic extracts were combined, dried (Na2SO4) and evaporated to give a bright yellow oil. This was purified by flash chromatography (silica flash) to give the title compound as a pale yellow solid. (0.8 g 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173061B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-976e7131d99e4023b98d49d0274e2994 |
| Source note | uspto-grants-2007_02 |