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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614265Generated: October 29, 2026

Chloride → Sodium methanethiolate

https://huagongshe.com/reaction/614265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantMethanethiolHCID 878—
ReactantAldoximeHCID 7863—
ReactantSodium HydroxideHCID 14798—
ReactantChlorineHCID 24526—
SolventEthylene GlycolHCID 174—
SolventWaterHCID 962—
ProductSodium methanethiolateHCID 4378561—
ProductHCID 20496527HCID 20496527—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Acetaldoxime (30 g., 0.5 mole) was dissolved in 200 g. of a solvent mixture containing 175 g. of water and 25 g. of ethylene glycol, and the solution was cooled to -5° to -10° C. Over a period of 20-30 minutes, 30 g. of chlorine was introduced to to the solution with good agitation. During chlorination, the reaction temperature was maintained at -5° to -10° C. An additional 6 g. of chlorine was added in 10 minutes. The mixture was stirred for 10-15 minutes at -10° C. A sodium methyl mercaptide solution was prepared by dissolving methyl mercaptan (25 g., 0.52 mole) in a caustic solution containing 40 g. of sodium hydroxide in 100 g. of water. The mercaptide solution was fed directly into the acethydroxamoyl chloride solution at -10° C. over a 15-20 minute period. The reaction mixture was stirred for an additional 15 minutes and then neutralized to pH 7.5 with a 50-percent caustic solution. The crystalline methyl hydroxythioacetimidate was recovered at -10° C. by filtration. The methyl hydroxythioacetimidate was reslurred in hexane, filtered and dried to obtain 47 gram of methylhydroxythioacetimidate mp 87°-89° C. This represented a 90% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04144261
Source datasetuspto-grants-1979_03
ORD IDord-d2e7be0bbfb0429fa0ec9cdb6e4de4e9
Source noteuspto-grants-1979_03