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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169232Generated: October 30, 2026

Acetic Anhydride → HCID 178476706, compound

https://huagongshe.com/reaction/2169232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178510888HCID 178510888—
SolventWaterHCID 962—
ProductHCID 178476706HCID 17847670642.94%

Reaction Steps

Ac2O (30 mL) was added to N-hydroxy-2-(3-phenyl-pyridin-2-yl)-acetamidine (160) (5.3 g, 23.35 mmol) at room temperature. A purple colored solution was formed, after a few hours a dark brown solution was formed which was stirred for 6 h at room temperature. Silica thin layer chromatography was performed (100% ethyl acetate, Rf=0.6). Cold water was added, the mixture was extracted with ethyl acetate (3×50 mL), the organic part was dried and concentrated, the crude product was purified by a CombiFlash column (eluted at 50% ethyl acetate in hexane) to get 2-(3-phenylpyridin-2-yl)ethanimidamido acetate (161) (2.7 g, 42.94% pure and 2 g mixture) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-47f0a1ede5084cf9ae40d49f6c1fa2c5
Source noteuspto-grants-2015_06