HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859337Generated: October 30, 2026
Potassium Carbonate → 7-Methoxy-3-(4-methoxyphenyl)thiochroman-4-one
https://huagongshe.com/reaction/1859337
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 10969180 | HCID 10969180 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Methoxy-3-(4-methoxyphenyl)thiochroman-4-one | HCID 11130368 | — |
Reaction Steps
To acetonitrile solution (120 ml) of 2-(4-methoxyphenyl)-3-(3-methoxyphenylthio)propionic acid (4) (12.8 g, 40.3 mmol) obtained above was added potassium carbonate (1.59 g, 11.5 mmol) and phosphorus oxychloride (18.7 ml, 200 mmol) at 0° C. and then stirred for 18 hours at 60° C. The reaction solution was quenched with ice-water and extracted with ether. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate and then distilled under reduced pressure to remove the solvent. The obtained crude product was washed with ether to obtain 6.8 g of the first crop of 7-methoxy-3-(4-methoxyphenyl)thiochroman-4-one (5). Further, the filtrate was concentrated and the residue was then purified with silica gel column chromatography (ethyl acetate:hexane=1:3) to obtain 1.0 g of the second crop of 7-methoxy-3-(4-methoxyphenyl)thiochroman-4-one (5) (total yield: 7.8 g, 65%). NMR data of the compound (5) was identical to that described in Example 25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06153768 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-0ad73b2939144917845e6748e62f173b |
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| Source note | uspto-grants-2000_11 |
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