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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489662Generated: November 2, 2026

Acetone → HCID 22902368, compound

https://huagongshe.com/reaction/1489662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22902353HCID 22902353—
ProductHCID 22902368HCID 22902368—

Reaction Conditions

Temperature-20 °C

Reaction Steps

7.3 g of 3-methoxyphenylthiobenzamide [preparation similar to Example 65B)] were dissolved in 50 ml acetone and cooled to -20° C. in a nitrogen atmosphere. A solution of 4 ml oxalyl chloride in 40 ml acetone were added slowly dropwise to this solution. Then it was stirred for 1 hour at 20° C. The crystals that settled out were drawn off and the mother liquor concentrated to approximately one-third of the original volume. A further crystal fraction was obtained. In all, 5 g of 2-(3-methoxyphenyl)-1,3-thiazole-4,5-dione were obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679699
Source datasetuspto-grants-1997_10
ORD IDord-72cecb65a15f435eaa5222fb4a2a6f7b
Source noteuspto-grants-1997_10