Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13745626 | HCID 13745626 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 13745627 | HCID 13745627 | — |
Reaction Steps
To a solution of 3-dimethylaminopropyl 4-[3-(4-acetyl-3-hydroxy-2-propylphenoxy)propoxy]-3-fluorobenzoate (124 mg) in dichloromethane (1 ml), triethylamine (0.5 ml) and 4-dimethylaminopyridine (a catalytic amount) was added acetic anhydride (0.38 ml). The mixture was stirred well for 1.5 hours at room temperature. To the reaction mixture was added methanol (2 ml), and the solvents removed by evaporation under reduced pressure. The residue was dissolved in chloroform, the solution was washed with a solution of saturated sodium hydrogen carbonate and dried with sodium sulfate, and the solvent was removed by evaporation. The residue was dissolved in ether, and to the solution was added a saturated solution of oxalic acid in ether until a precipitate did not emerge any more. The precipitate was recovered by filtration and washed with ether to give a white solid of 3-dimethylaminopropyl 4-[3-(3-acetoxy-4-acetyl-2-propylphenoxy)propoxy]-3-fluorobenzoate.mono-oxalate (180 mg). M.p. 166°-167° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04714774 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-111e7588e2404d309c4a7a44f8c7ac21 |
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| Source note | uspto-grants-1987_12 |
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