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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085804Generated: October 30, 2026

Dimethyl Sulfide → HCID 13366864, compound

https://huagongshe.com/reaction/1085804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantDimethyl SulfateHCID 6497—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 20059007HCID 20059007—
SolventAcetonitrileHCID 6342—
ProductHCID 13366864HCID 1336686498.2%

Reaction Steps

A solution of 9.8 g (0.77 mole) of dimethyl sulphate and 5.3 g (0.085 mole) of dimethyl sulphide in 50 ml of acetonitrile is stirred at room temperature for 5 days. A solution of 13 g (0.044 mole) of 4-chlorophenyl-tert.butyl 1-(1,2,4-triazol-1-yl)-ethyl ketone in 20 ml of acetonitrile is then added dropwise at room temperature. At the same temperature, 4.8 g (0.088 mole) of sodium methylate are introduced and the mixture is subsequently stirred for 20 hours and then concentrated in vacuo. The residue is stirred overnight with a mixture of 35 ml of ethyl acetate and 25 ml of water. The organic phase is separated off, dried over sodium sulphate and concentrated in vacuo. 13.2 g (98.2% of theory) of 2-(4-chlorophenyl-tert.-butyl)-2-[1-(1,2,4-triazol-1-yl)-ethyl]oxirane of refractive index nD20 1.5431 are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011850
Source datasetuspto-grants-1991_04
ORD IDord-ebfc2a0721584bb1aa1901b40c1d3d31
Source noteuspto-grants-1991_04