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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544504Generated: October 26, 2026

2-Mercaptoethanol → HCID 13341318, compound

https://huagongshe.com/reaction/544504

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
ReactantPotassium HydroxideHCID 14797—
Reactant1H-Pyrazole, 3,4,5-trichloro-1-methyl-HCID 1475184—
Catalyst18-Crown-6HCID 28557—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 13341318HCID 1334131838.1%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a mixture of 26.5 g (0.34 moles) 2-mercaptoethanol, 19 g of 85% potassium hydroxide, and a few drops of 18-Crown-6 in 250 ml of DMSO, 60 g(0.32 moles) 1-methyl-3,4,5-trichloro pyrazole (product of Example 1 or 1A)were added in portions. When the addition was complete, the reaction mixture was heated to 140° C. for 1 day. The cooled reaction mixture was diluted with water and extracted with ether. The oganic phase was washed four times with 200 ml water per time, dried and stripped. The crude product was chromatographed on a silica gel column. The product, 1-methyl-3,4-dichloro-5-(2-hydroxyethyl) thio pyrazole, was eluted from the column with ethyl acetate, yielding 27.7 g (37.7% yield) of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04450278
Source datasetuspto-grants-1984_05
ORD IDord-fc654e7391d84b03a495bd43d9d35517
Source noteuspto-grants-1984_05