HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → HCID 131714937, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoate | HCID 600916 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 131714937 | HCID 131714937 | 76% |
Reaction Steps
To 3.0 g (11.33 mmol) of 2-(2,3,4,5-tetrafluorobenzoyl)acetic acid, ethyl ester was added 2.49 g of triethylorthoformate and 2.76 g of acetic anhydride. The mixture was refluxed for two hours and was concentrated under high vacuum at 80° C. to dryness. The residual oil was treated with 1.05 g (1.0 equivalent) of aniline dissolved in 70 ml of isopropyl alcohol. After 24 hours the mixture was concentrated and the solid triturated with hexane. Filtration gave 2.88 g of 2,3,4,5,-tetrafluoro-β-oxo-α-1-ethoxyethylidene-phenylpropanoic acid, ethyl ester, mp 101°-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04617308 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-c64ca49d22a84d3cb84131e66b637891 |
| Source note | uspto-grants-1986_10 |