Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Anisole | HCID 7519 | — |
| Reactant | 2-Chloro-3-methylbenzoyl chloride | HCID 19367940 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53953369 | HCID 53953369 | 97% |
Reaction Steps
A solution of 2-chloro-3-methylbenzoyl chloride (18.05 mmol), [prepared as described above] in dry CH2Cl2 (60 ml) was cooled to 0° C. and AICl3 (2.41 g, 1 eq.) was added. After ten minutes, anisole (1.96 ml, 1 eq.) was added. The resulting orange colored reaction mixture was allowed to warm to room temperature, stirred for 3 h and then poured on ice. The product was extracted into ether, washed with brine, and dried over MgSO4 . The solvent was evaporated in vacuo to give 3-(4-methoxybenzoyl)-2-chlorotoluene (4.55 g, 97% yield) as a solid, mp 64.7°-65.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05886178 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-a1b2805c9a9443f9b71e39b049c4ad63 |
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| Source note | uspto-grants-1999_03 |
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