Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 1-Benzylpiperidine | HCID 76190 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 54135013 | HCID 54135013 | 80% |
Reaction Steps
A solution of n-butyllithium in toluene (20%; 65.6 g; 0.20 mol) is added over the course of from 10 to 15 min to a solution of 31 g of N-benzylpiperidine (0.175 mol) in 60 ml of tert-butyl methyl ether. The reaction mixture is heated at from 55° to 60° C. for approximately 18 h and then metered at RT into a cold (-20° C.) solution of 50.1 g of diethyl oxalate (0.42 mol) in 160 ml of toluene. The mixture is heated to RT and stirred at from 20° to 25° C. for 30 min. Acetic acid (100%; 12.6 g; 0.21 mol) and a mixture of 50 g of crushed ice and 100 g of water are then added to the reaction mixture. The phases are separated and the organic phase is washed with 50 ml of water and concentrated by evaporation in vacuo: 43.2 g (content 89%; yield 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05756811 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-e8803f2b00bc4e758b71eb2464a3944f |
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| Source note | uspto-grants-1998_05 |
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