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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700039Generated: October 30, 2026

Acetic Anhydride → HCID 10931553, compound

https://huagongshe.com/reaction/1700039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Reactant2-METHOXY-3-BUTEN-1-OLHCID 2735078—
SolventTolueneHCID 1140—
ProductHCID 10931553HCID 10931553—

Reaction Conditions

Temperature60 °C

Reaction Steps

In a 3-liter, 3-necked round bottom flask equipped with a mechanical stirrer, nitrogen inlet, temperature probe and vigoreux column was placed 1200 mL toluene, sodium acetate (88.59 g, 1.08 mol) and 2-methoxy-3-buten-1-ol (250.0 g, 2.45 mol). Mixture heated to 60° C. with stirring. Once temperature had stabilized, acetic anhydride (288.83 g, 2.80 mol) added dropwise over 2.5 hours. Maintained temperature for 1.5 hrs then increased temperature to 70° C. for 1 hour. Gas chromatography showed no trace of starting material in reaction. Began cooling reaction to room temperature. When reaction had cooled to 38° C., one liter of a 5% sodium bicarbonate solution was added at high speed to decompose any excess acetic anhydride remaining in the reaction. Extracted reaction twice with water, layers separated, the aqueous layer extracted twice with toluene and added to the organic layer. Organic layer dried with anhydrous magnesium sulfate, filtered and concentrated by rotovap. Yield 222.43 g (63.0%) of a clear, colorless material. 1H NMR consistent with 1-acetoxy-2-methoxy butene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348623B2
Source datasetuspto-grants-2002_02
ORD IDord-005a4fbd081246e4bc7b07567e8732be
Source noteuspto-grants-2002_02