HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Ethyl 2-(2,4,5-trifluoro-6-methylbenzoyl)-3-ethoxyacrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | HCID 86750081 | HCID 86750081 | — |
| Product | Ethyl 2-(2,4,5-trifluoro-6-methylbenzoyl)-3-ethoxyacrylate | HCID 54242925 | — |
Reaction Steps
A solution of 7.1 g (27 mmol) of ethyl (3-2 (2,4,5-trifluoro-6-methylbenzoyl)-β-oxopropanoate, 6.8 g (41 mmol) of triethyl orthoformate and 60 mL of acetic anhydride was refluxed for 3 hours, cooled to room temperature, and concentrated to give 8.4 g of the title compound. The crude material was used as is in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05585491 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-70bed5b2a1df43ada72b6a80f88e8e43 |
| Source note | uspto-grants-1996_12 |