HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561168Generated: October 31, 2026
Acetic Anhydride → HCID 178472004, compound
https://huagongshe.com/reaction/561168
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-Amino-1-butanol | HCID 25868 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Ethyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoate | HCID 600916 | — |
| Product | HCID 178472004 | HCID 178472004 | 97.2% |
Reaction Steps
A mixture of ethyl 2,3,4,5-tetrafluorobenzoylacetate (2.64 g, 10.0 mmol), Ac2O (2.36 mL, 25.0 mmol) and triethyl orthoformate (2.49 mL, 15.0 mmol) was stirred at 130° C. for 3 h. The mixture was concentrated in vacuo and dried under high vacuum. The crude product was dissolved in EtOH (50 mL) and 4-amino-1-butanol (0.972 mL, 10.5 mmol) was added. After stirred at room temperature for 17 h, the mixture was concentrated in vacuo and the crude product was purified by column chromatography (Hexane:EtOAc 2:1→1:2) to yield ethyl 3-(4-hydroxybutylamino)-2-(2,3,4,5-tetrafluorobenzoyl)acrylate (3.53 g, 97%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08063221B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-5fce5efe24684caaa2bfa9a38084cc0c |
|---|
| Source note | uspto-grants-2011_11 |
|---|