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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561168Generated: October 31, 2026

Acetic Anhydride → HCID 178472004, compound

https://huagongshe.com/reaction/561168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Amino-1-butanolHCID 25868—
ReactantEthyl orthoformateHCID 31214—
ReactantEthyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—
ProductHCID 178472004HCID 17847200497.2%

Reaction Conditions

Temperature130 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063221B2
Source datasetuspto-grants-2011_11
ORD IDord-5fce5efe24684caaa2bfa9a38084cc0c
Source noteuspto-grants-2011_11