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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279611Generated: October 31, 2026

Acetic Anhydride → HCID 44185486, compound

https://huagongshe.com/reaction/2279611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
ReactantButanoic acid, 4,4-difluoro-3-oxo-, ethyl esterHCID 67697—
ProductHCID 44185486HCID 44185486—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of ethyl 4,4-difluoro-3-oxobutanoate (4.65 g, 0.028 moles), acetic anhydride (8.0 g, 0.078 moles) and triethylorthoformate (7.3 g, 0.049 moles) is heated at 110° C. for 4 h. The mixture is concentrated under vacuum to afford (Z)-ethyl 2-(ethoxymethylene)-4,4-difluoro-3-oxobutanoate as yellow oil. The oil is dissolved in EtOH (25 mL) and cooled in an ice bath. To this cooled stirred mixture is added anhydrous hydrazine (0.7 mL, 0.022 mole) and the mixture is allowed to warm gradually to RT overnight. The mixture is concentrated under vacuum and the crude product is purified by silica gel column chromatography using 1-2% MeOH/CH2Cl2 to afford the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133204B2
Source datasetuspto-grants-2015_09
ORD IDord-b04f98a0f5884a85b652bd58460f8cf1
Source noteuspto-grants-2015_09