HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277757Generated: October 26, 2026
Methyl iodide → Methyl alpha-methylthio-alpha-(m-phenoxyphenyl)propionate
https://huagongshe.com/reaction/1277757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl alpha-methylthio(m-phenoxyphenyl)acetate | HCID 20556696 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl alpha-methylthio-alpha-(m-phenoxyphenyl)propionate | HCID 12917662 | 94% |
Reaction Steps
Methyl α-methylthio(m-phenoxyphenyl)acetate (1.963 g) was dissolved in anhydrous dimethylformamide, and under ice cooling, 280 mg (65% content) of sodium hydride was added. The mixture was stirred for 10 minutes. Then, 0.60 ml of methyl iodide was added, and the mixture was stirred under ice cooling for 5 minutes and then at room temperature for 30 minutes. After adding an aqueous solution of ammonium chloride (500 mg/40 ml), the reaction mixture was extracted three times with 20 ml of diethyl ether. The organic layer was washed three times with 10 ml of water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was chromatographed on a silica gel column using hexane and benzene as eluents to afford 1.930 g of methyl α-methylthio-α-(m-phenoxyphenyl)propionate as an oil in a yield of 94%. Distillation of this substance gave a fraction boiling at 147°-149° C./0.08 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04278802 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-3593426b84354911a822642d5c807fb0 |
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| Source note | uspto-grants-1981_07 |
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