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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-Chloropyruvaldehyde-1-[2,6-dichloro-4-(trifluoromethyl)-phenyl]hydrazone | HCID 131718235 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Methylthio)pyruvaldehyde-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]hydrazone | HCID 131718236 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05258523 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-d4069e1577554c3c9d6b2cf6e71d9989 |
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| Source note | uspto-grants-1993_11 |
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