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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606252Generated: October 31, 2026

Dichloromethane → HCID 73794030, compound

https://huagongshe.com/reaction/1606252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantIsobutyronitrileHCID 6559—
ReactantSodium hydrideHCID 24758—
ReactantMethyl (methylsulfinyl)methyl sulfideHCID 99129—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 73794030HCID 7379403072.3%

Reaction Steps

1.78 Grams of methyl methylthiomethyl sulfoxide was dissolved in 20 ml of THF, and to which 375 mg of sodium hydride was added under cooling with ice, followed by 30 minutes' stirring at room temperature. Thereafter 1.6 ml of isobutyronitrile was added and stirred for 16 hours at room temperature, and for 6 hours at 50°C., followed by further addition of 70 ml of methylene chloride and 2 ml of water, and subsequent an hour's stirring at room temperature. The reaction mixture was dried with Glauber's salt, and concentrated under reduced pressure to leave a yellow solid. Washing the solid with a carbon tetrachloride-n-hexane system, 1.525 g of 1-methylsulfinyl-1-methylthio-2-amino-3-methyl-1-butene was obtained as a light yellow solid. The washing was concentrated under reduced pressure, and subjected to a column chromatography (silica gel, methylene chloride, ethyl acetate, and methanol) to allow the recovery of 117 mg of methyl methylthiomethyl sulfoxide and 480 mg of 1-methylsulfinyl-1-methylthio-2-amino- 3-methyl-1-butene. The isolation yield was 72.3%, and the conversion yield was 77.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952044
Source datasetuspto-grants-1976_04
ORD IDord-2750bc027b2a46fe92e6b8342072c39a
Source noteuspto-grants-1976_04