Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | p-(Trifluoromethoxy)benzaldehyde | HCID 69573 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 4361347 | HCID 4361347 | 92.4% |
Reaction Steps
A mixture of N-acetylglycine (5.00 g, 42.7 mmol), 4-trifluoromethoxybenzaldehyde (9.30 g, 47.0 mmol), sodium acetate (4.55 g, 55.5 mmol), and acetic anhydride (20 mL, 213 mmol) was stirred at 120° C. for 1 hour, and then was cooled to room temperature. After further ice-cooling, the precipitated yellow solid was suspended in water. The insoluble substance was collected by filtration, washed with water, and dried by heating under reduced pressure to give 10.7 g of the title compound (yellowish brown crystal, yield: 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08344029B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-c4a63c51f74e427fa6f71d6de79dfdf7 |
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| Source note | uspto-grants-2013_01 |
|---|