Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117888Generated: November 1, 2026

Acetic Anhydride → HCID 21914847, compound

https://huagongshe.com/reaction/2117888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetylglycineHCID 10972—
Reactant4-(Methylthio)benzaldehydeHCID 76985—
ReactantSodium AcetateHCID 517045—
SolventEthyl AcetateHCID 8857—
ProductHCID 21914847HCID 2191484736.5%

Reaction Steps

4-(Methylsulfanyl)benzaldehyde (31.8 g), (acetylamino)acetic acid (24.5 g) and acetic anhydride (35 ml) were combined, and then sodium acetate (8.57 g) was added to the suspension at room temperature under nitrogen atmosphere. The reaction mixture was refluxed for 3.5 hours. After cooled to room temperature, the mixture was poured into ice-water and ethyl acetate with stirring, and filtered in vacuo. The filtrate was separated. The organic layer was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue and the previously obtained solid were combined, and the mixture was purified by flash column chromatography over silica gel with chloroform/ethyl acetate (30:1) as an eluent, and triturated with isopropyl ether to give (4Z)-2-methyl-4-(4-(methylsulfanyl)benzylidene)-1,3-oxazol-5(4H)-one (17.8 g) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442715B2
Source datasetuspto-grants-2008_10
ORD IDord-36e0f5d88aed405bb7e7e2a59450131c
Source noteuspto-grants-2008_10