Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | 1-(chloromethyl)-2-ethoxybenzene | HCID 2530231 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67856346 | HCID 67856346 | — |
Reaction Steps
A Grignard solution of 30.5 g of 2-ethoxybenzyl chloride and 6.1 g of magnesium shavings in 250 ml of diethyl ether is added dropwise at -60° C. to -70° C. to 50 ml of sulfur dioxide. Stirring is continued for 0.5 hour at -70° C., the mixture is allowed to come to room temperature, and the salt magnesium 2-ethoxybenzylsulfinate which has formed (47 g, melting point: 134°-139° C., decomposition) is filtered off with suction. The sulfinate salt is dissolved in 900 ml of water and 16.4 g of anhydrous sodium acetate. To this are added 22.7 g of hydroxylamine-O-sulfonic acid at room temperature with stirring. After the mixture has been stirred for 12 hours, the product is filtered off with suction and dried in vacuo. This gives 23.9 g of 2-ethoxybenzylsulfonamide of melting point: 92°-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05053072 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-6781643c2f7540f0b65348b3ee2aa6f8 |
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| Source note | uspto-grants-1991_10 |
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