HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569707Generated: October 30, 2026
Dimethyl Sulfide → HCID 13254742, compound
https://huagongshe.com/reaction/569707
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 13254741 | HCID 13254741 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13254742 | HCID 13254742 | 80.4% |
Reaction Steps
A solution of 41.9 ml (0.567 mol) of dimethyl sulphide in 50 ml of acetonitrile was added dropwise to a solution of 49.4 ml (0.518 mol) of dimethyl sulphate in 250 ml of acetonitrile at 25° C., in the course of 2 hours, with external cooling. After the mixture had stood for 4 days at room temperature, 87.4 g (0.31 mol) of 5-(biphenyl-4-yloxy)-3,3-dimethylpent-1-en-4-one, dissolved in 90 ml of acetonitrile, were stirred in in the course of 1 hour. Thereafter, 31.6 g (0.58 mol) of sodium methylate were introduced at 25° C. After the mixture had been stirred for twelve hours at room temperature, the precipitated salt was filtered off, and the filtrate was concentrated. The oily residue was taken up in 500 ml of ethyl acetate, and the solution was washed with twice 500 ml of water and dried over anhydrous sodium sulphate. After the solution had been concentrated in vacuo, 73.4 g (80.4% of theory) of 2-(biphenyl-4-yloxymethyl)-2-(3,3-dimethylprop-1-en-3-yl)-oxirane were obtained as a colorless waxy mass. ##STR23##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04734126 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-b5a4f18358094fe8a2e873fe10598361 |
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| Source note | uspto-grants-1988_03 |
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