HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267778Generated: October 31, 2026
Water → 7-Methoxy-3-(4-methoxyphenyl)-3-(2-propenyl)thiochroman-4-one
https://huagongshe.com/reaction/1267778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 7-Methoxy-3-(4-methoxyphenyl)thiochroman-4-one | HCID 11130368 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 7-Methoxy-3-(4-methoxyphenyl)-3-(2-propenyl)thiochroman-4-one | HCID 18546281 | 79% |
Reaction Steps
Allyl bromide (5.7 ml, 66.56 mmol) was added dropwise to a solution of 7-methoxy-3-(4-methoxyphenyl)thiochroman-4-one (2 g, 6.64 mmol) in dimethyl sulfoxide (34 ml). To this mixture, a solution of potassium tert-butoxide (5.22 g, 46.55 mmol) in dimethyl sulfoxide (70 ml) was slowly added dropwise at 10° C., followed by stirring for 2 hours at 10° C. and for 15 hours at room temperature. Water was added to the reaction mixture, which was then extracted three times with ethyl acetate. The combined organic layers were washed with water and saturated aqueous sodium chloride, and then dried over anhydrous magnesium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluent:ethyl acetate/hexane=1/9) to give 7-methoxy-3-(4-methoxyphenyl)-3-(2-propenyl)thiochroman-4-one (1.78 g, Yield 79%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552068B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-5df879eace7e4b829809aad12e653c20 |
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| Source note | uspto-grants-2003_04 |
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