HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949133Generated: October 31, 2026
Methanol → 2-(3,4-Dichlorophenyl)-3-hydroxy-4-methylcarbonyl-2,5-dihyrothiophene
https://huagongshe.com/reaction/1949133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate | HCID 58281519 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3,4-Dichlorophenyl)-3-hydroxy-4-methylcarbonyl-2,5-dihyrothiophene | HCID 44207040 | 69.3% |
Reaction Steps
A methanol (500 mL) solution of sodium amide (19.2 g, purity: 90%, 1.5 equivalent amounts based on the starting material) was heated to 40° C., and to this solution, a methanol (200 mL) solution of methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate (100 g, purity: 95%, 296 mmol) was dropwise added over a period of 12 minutes, followed by stirring at 40° C. for 1 hour. The reaction solution was cooled to 5° C., water (300 mL) was dropwise added over a period of 10 minutes, and then the solvent was distilled off. To the obtained crude product, chloroform and a saturated ammonium chloride aqueous solution were added, followed by liquid separation, and the organic layer was washed with a saturated salt solution and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off to give the desired product as an oil (59.3 g, yield: 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399685B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-ab7b960c34b94f909af9147d38110052 |
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| Source note | uspto-grants-2013_03 |
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