Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Product | HCID 1653334 | HCID 1653334 | — |
Reaction Steps
In a 500 mL round bottom flask, fitted with a reflux, condenser, succinic anhydride (10.03 g, 1.2 eq.) and dimethylaminopyridine (10.2 g, 1 eq.) and benzyl alcohol (9.01 g, 1 eq.) in MTBE (250 mL) were combined. The reaction mixture was placed under inert atmosphere and stirred in an oil bath at 68° C. for 4 hours. The reaction was then quenched with a solution of 10% NaHCO3 and extracted with MTBE. The organic layer was washed with NaHCO3 and brine. The organic layer was collected, dried using MgSO4, and concentrated to give a white solid. The crude product was purified using column chromatography to give 14.1 g of white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07959958B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-765a239e316a442e83596c6ca62eee75 |
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| Source note | uspto-grants-2011_06 |
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