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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396078Generated: October 26, 2026

Acetic Anhydride → HCID 178471966, compound

https://huagongshe.com/reaction/1396078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
Reactant1-AminocyclopentanemethanolHCID 66307—
ReactantEthyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—
ProductHCID 178471966HCID 17847196690.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of ethyl 3-oxo-3-(2,3,4,5-tetrafluorophenyl)propionate (3.17 g, 12 mmol), acetic anhydride (3.34 mL, 3.6 g, 30 mmol) and triethyl orthoformate (3.00 mL, 2.6 g, 18 mmol) was heated at 130° C. for 1.5 h. The mixture was concentrated in vacuo and dried under high vacuum for 3 hours. The crude product was dissolved in EtOH (15 mL) and cooled to 0° C. and then 1-amino-1-cyclopentanemethanol (1.01 g, 8.8 mmol) was added very slowly. After 1.5 h, the solvent was removed by evaporation to yield the title compound as yellow oil (3.1 g crude) that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901112B2
Source datasetuspto-grants-2014_12
ORD IDord-2e0aeb17d72e49cbb67526d3578b1b4e
Source noteuspto-grants-2014_12