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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544661Generated: November 3, 2026

Water → HCID 20458352, compound

https://huagongshe.com/reaction/544661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 20458355HCID 20458355—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 20458352HCID 20458352—

Reaction Steps

5.75 g of 2-[4,5-bis-(p-methoxyphenyl)-thiazol-2-ylsulphinyl]-acetaldehyde-dimethylacetal are dissolved in 5 ml of acetic acid. Then, while stirring, 30 ml of a mixture of 2 parts acetic acid, 1 part sulphuric acid and 1 part water are added dropwise over a period of 5 minutes. The mixture is stirred at room temperature for 30 minutes, diluted with 100 ml of methylene chloride and poured into 200 ml of ice-water. The organic layer is removed and washed with 200 ml of ice-water. The aqueous phase is extracted by shaking three times with 50 ml of methylene chloride each time. The organic phases are combined, dried over magnesium sulphate and concentrated to dryness by evaporation. The crude product is dissolved in 200 ml of methylene chloride and stirred with 5 g of silica gel. The mixture is filtered, concentrated to dryness by evaporation and dried under reduced pressure. 2-[4,5-bis-(p-methoxyphenyl)-thiazol-2-ylsulphinyl]-acetaldehyde is obtained in the form of a highly viscous oil, IR-spectrum: νC=O =1720 cm-1, νS=O =1080 cm-1 (CCl4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04451471
Source datasetuspto-grants-1984_05
ORD IDord-00d41836222b4b7cbc6c98fb717bdb6c
Source noteuspto-grants-1984_05