HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249395Generated: November 3, 2026
Dimethyl Sulfoxide → HCID 13532506, compound
https://huagongshe.com/reaction/1249395
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | HCID 13532505 | HCID 13532505 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13532506 | HCID 13532506 | — |
Reaction Steps
1.5 g (0.05 mol) of 80% pure sodium hydride are added in portions to a mixture of 11 g (0.05 mol) of trimethylsulphoxonium iodide and 60 ml of dimethylsulphoxide at 10° C., with stirring. The reaction mixture is stirred for 15 minutes, 17.7 g (0.05 mol) of 3-(4-chlorobenzyloxy)-(6-chloropyridin-2-yloxy)-3-methyl-2-butanone in a little dimethylsulphoxide are then added dropwise and the mixture is warmed at 60° C. for 1 hour. It is subsequently poured into water, under a nitrogen atmosphere, and extracted with methylene chloride. The organic phase is dried over sodium sulphate and concentrated. The crude 2-[2-(4-chlorobenzyloxy)-prop-2-yl]-2-(6-chloropyridin-2-yloxymethyl)-oxirane thus obtained is further reacted directly. ##STR13##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04631288 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-f409a5f2a1cc4bafb2c88f5da30c4ee0 |
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| Source note | uspto-grants-1986_12 |
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