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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195902Generated: October 31, 2026

Hydrochloric Acid → HCID 54354349, compound

https://huagongshe.com/reaction/1195902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 53925475HCID 53925475—
SolventPotassium HydroxideHCID 14797—
ProductHCID 54354349HCID 5435434983.5%

Reaction Steps

5 g of 2-(2-chlorophenoxymethyl)-phenylglyoxylic acid methyl ester O-methyloxime in 50 ml of 1N aqueous KOH solution were refluxed for 2 hours. The mixture was cooled, after which the pH was brought to 1 with concentrated hydrochloric acid. The precipitate which separated out was filtered off under suction and dried. 4 g of 2-(2-chlorophenoxymethyl)-phenylglyoxylic acid O-methyloxime were obtained as a colorless solid, which was then dissolved in 50 ml of anhydrous dimethylformamide. 2.1 g of carbonyldiimidazole were added at -10° C. and stirring was carried out at this temperature for 2 hours. 0.89 g of sodium methanethiolate was then added and stirring was continued for a further 90 minutes at -10° C. and then for a further 90 minutes at room temperature. 100 ml of methylene chloride and 200 ml of saturated, aqueous sodium chloride solution were added, after which the organic phase was separated off and dried over magnesium sulfate and the solvent was removed under reduced pressure. 3.8 g of crude product were obtained. This was purified by flash chromatography over silica gel using hexane/ethyl acetate, 2.3 g of product being obtained as a yellow solid of melting point 58° to 60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112860
Source datasetuspto-grants-1992_05
ORD IDord-d034cdb6118b43a1850ccb611d54659f
Source noteuspto-grants-1992_05