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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606253Generated: October 30, 2026

Dichloromethane → HCID 73794037, compound

https://huagongshe.com/reaction/1606253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBenzonitrileHCID 7505—
ReactantSodium hydrideHCID 24758—
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 73794037HCID 7379403766%

Reaction Steps

4.38 Grams of methyl methylthiomethyl sulfoxide was dissolved in 45 ml of THF, and to the solution 900 mg of sodium hydride was added under cooling with ice, and the system was stirred for an hour at room temperature. Upon addition of 4 ml of benzonitrile and subsequent stirring for 42.5 hours at room temperature, the entire system was solidified, to which 100 ml of methylene chloride and 3 ml of water were added, followed by 30 minutes' stirring and then drying with Glauber's salt. The light yellow solid obtained by the subsequent concentration under reduced pressure was washed with 100 ml of carbon tetrachloride, and 5.158 g of 1-methylsulfinyl-1-methylthio-2-amino-2-phenylethylene was obtained as a light yellow solid. The washing was concentrated under reduced pressure, and subjected to a column chromatography (silica gel, ethyl acetate, and methanol) to allow the recovery of 1.106 g of a light yellow, oily substance. Upon NMR analysis, the oily substance was confirmed to be composed of 972 mg of methyl methylthiomethyl sulfoxide and 134 mg of 1-methylsulfinyl-1-methylthio-2-amino-2-phenylethylene. The latter's isolation yield was 66%, and the conversion yield was 84.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952044
Source datasetuspto-grants-1976_04
ORD IDord-6e41fb6521d84d2680dae041035a7766
Source noteuspto-grants-1976_04