Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | monoMethyl succinate | HCID 77487 | — |
| Reactant | HCID 605592 | HCID 605592 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 18977146 | HCID 18977146 | 84.6% |
Reaction Steps
45.9 g of oxalyl chloride and 5 drops of dimethylformamide were added to a dichloroethane solution (500 ml) containing 45.5 g of methyl hydrogen succinate, and the mixture was stirred at room temperature for 3 hours. Under ice cooling, a dichloroethane solution (60 ml) containing 31.3 g of [4-(acetylamino)butyl]benzene, and 91.9 g of anhydrous aluminum chloride were added thereto, and the mixture was stirred for 1 hour. The reaction mixture was poured into ice water, and the organic layer was collected by separation. After the organic layer was washed with water and dried, the solvent was removed. The resulting crude crystal was recrystallized from ethyl acetate to obtain 42.3 g of 4-[4-(acetylamino)butyl]-l-(3-methoxycarbonylpropionyl)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05698554 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-2f0ad92b1ff6422a884e1a4fd2fac2a5 |
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| Source note | uspto-grants-1997_12 |
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