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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592947Generated: October 30, 2026

Acetic Anhydride → HCID 86592830, compound

https://huagongshe.com/reaction/1592947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,3-diethoxyacetoneHCID 227346—
ReactantHCID 178462451HCID 178462451—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86592830HCID 8659283097.6%

Reaction Steps

A solution (360 mL, 180 mmol) of ethynyl magnesium chloride in 0.5 M THF was stirred under ice-cooling and 1,3-diethoxyacetone (21.93 g, 150 mmol) was added dropwise. The mixture was stirred under ice-cooling for 30 min and acetic anhydride (18.4 mL, 195 mmol) was added dropwise. The mixture was stirred at room temperature for 1 hr. After the completion of the reaction, aqueous ammonium chloride solution was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous magnesium sulfate and concentrated to give acetic acid 1,1-bis-ethoxymethyl-2-propynyl ester (31.36 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07294629B2
Source datasetuspto-grants-2007_11
ORD IDord-21b0ac09a2d34e7eb9ca8e122e9c48fe
Source noteuspto-grants-2007_11