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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714417Generated: November 2, 2026

Acetic Anhydride → HCID 66693303, compound

https://huagongshe.com/reaction/714417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 66692810HCID 66692810—
SolventTolueneHCID 1140—
ProductHCID 66693303HCID 66693303—

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of 1-cyclopropyl-3-(1,6-dihydro-6-oxo-1,2-diphenyl-5-pyrimidinyl)-1,3-propanedione (i.e. the product from Example 6, Step A) (165 mg, 0.46 mmol), triethyl orthoformate (0.23 mL, 1.4 mmol), and acetic anhydride (0.92 mL) was heated at 110° C. under a nitrogen atmosphere for 4 h. The residue was dissolved in toluene (5 mL) and the resulting solution was concentrated under reduced pressure at 50° C. The residue was re-dissolved in toluene (5 mL) and the resulting solution was concentrated at 50° C. to give 181 mg of the title compound as a brown oil that was used in the next step without further purification. 1H NMR analysis showed the product to contain a mixture of Z- and E-olefin isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187432B2
Source datasetuspto-grants-2015_11
ORD IDord-5cd37c9029db476598ddfc1c8e2b4efe
Source noteuspto-grants-2015_11