Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Syringaldehyde | HCID 8655 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Product | HCID 4767934 | HCID 4767934 | 31.7% |
Reaction Steps
A 1.8 g (9.88 mmol) of syringaldehyde, 1.4 g (12.0 mmol) of N-acetylglycine, 1 g (12.2 mmol) of sodium acetate and 5 ml of acetic anhydride were stirred at 120° C. for 6 hours. A precipitate was washed with water and ethanol in this order and dried under reduced pressure. To the product was added 80 ml of 0.1N hydrochloric acid, and the mixture was stirred at 90° C. for 1 hour. A crystal formed was washed with water and acetone in this order to give 880 mg (yield 31.7%) of objective αacetylamino-3,5-dimethoxy-4-hydroxycinnamic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05478856 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-2f23e983c60a4576af9eb206b4d653da |
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| Source note | uspto-grants-1995_12 |
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