HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255397Generated: October 29, 2026
Dimethyl Sulfoxide → HCID 19738046, compound
https://huagongshe.com/reaction/2255397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2-Methoxyphenyl)acetonitrile | HCID 81496 | — |
| Reactant | 2-(Bromomethyl)tetrahydro-2H-pyran | HCID 141917 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19738046 | HCID 19738046 | 82% |
Reaction Steps
To a flask was added 20 g. (0.1346 mole) of (2-methoxyphenyl)acetonitrile, 25 g. (0.1346 mole) of 2-(bromomethyl)tetrahydro-2H-pyran, and 200 ml. of DMSO. The mixture was stirred for five minutes at room temperature and to the resultant solution was added 22 g. (0.2692 mole) of 50% aqueous sodium hydroxide over 30 minutes with the reaction temperature being allowed to exotherm to 60° C. The reaction was stirred an additional two hours, then cooled, water added and the organic material extracted with ether. The combined ether extracts were then washed with water, dried, filtered, and the ether distilled. The organic residue wss fractionally distilled to obtain 27 g. (82% yield) of the 2-(2-methoxyphenyl)-3-(tetrahydropyran-2-yl)propionitrile boiling 145°-160° C. at 5 mm of Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05240925 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-eda1257f3b7c44ac8914353154a60b15 |
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| Source note | uspto-grants-1993_08 |
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