Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Veratrole | HCID 7043 | — |
| Reactant | Benzoyl chloride, 2-chloro-5-nitro- | HCID 117637 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | HCID 10591888 | HCID 10591888 | 78% |
Reaction Steps
2-Chloro-5-nitrobenzoyl chloride (11 g; 0.05 mole), 1,2-dimethoxybenzene (20 ml; 0.15 mole) and anhydrous ferric chloride (0.5 g) are successively introduced into a flask. The mixture is progressively heated to 150° C., and maintained at this temperature for 1 hour. After cooling, the reaction mixture is poured into 1N HCl (200 ml), then extracted with dichloromethane (3×200 ml). After washing with a sodium bicarbonate solution, the organic phase is dried over MgSO4 and then concentrated under reduced pressure to provide a brown oil. By trituration with pentane (300 ml), 2-chloro-3',4'-dimethoxy-5-nitrobenzophenone (12.5 g; yield: 78%) is isolated in the form of a beige solid of m.p. 138° C. (compound no. 171).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05342835 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-f6576afe7ace48f5b3c6ca8be2b5d9ab |
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| Source note | uspto-grants-1994_08 |
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