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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256727Generated: October 31, 2026

Methanethiol → 3-(Methylthio)pyruvaldehyde-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]hydrazone

https://huagongshe.com/reaction/256727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Chloropyruvaldehyde-1-[2,6-dichloro-4-(trifluoromethyl)-phenyl]hydrazoneHCID 131718235—
SolventMethanolHCID 887—
Product3-(Methylthio)pyruvaldehyde-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]hydrazoneHCID 131718236—

Reaction Conditions

Temperature40 °C

Reaction Steps

9.2 g of sodium was dissolved in 900 ml of methanol. 21.3 g of methanethiol was introduced into the sodium methylate solution thus obtained. Then 110.0 g of 3-chloropyruvaldehyde-1-[2,6-dichloro-4-(trifluoromethyl)-phenyl]hydrazone (produced according to Example 1) was added in portions at 30° to 40° C. The reaction mixture was stirred for 1 hour at 40° C. and then the methanol was distilled off in a water jet vacuum. The residue was mixed with 500 ml of water and extracted three times with 250 ml of dichloromethane each. The combined dichloromethane extracts were dried on sodium sulfate and concentrated by evaporation. The residue was suspended in 200 ml of n-hexane, filtered off and dried in a water jet vacuum. The yield of the product was 92.2 g [content (GC): 94.7 percent]. The melting point of the product was 88° to 90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258523
Source datasetuspto-grants-1993_11
ORD IDord-d4069e1577554c3c9d6b2cf6e71d9989
Source noteuspto-grants-1993_11