Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Methoxybenzylamine | HCID 81292 | — |
| Reactant | HCID 13333282 | HCID 13333282 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21487306 | HCID 21487306 | — |
Reaction Steps
43 g of 2,4-diphenoxy-5-sulfamoyl-benzoic acid (0.1 mol) prepared according to Example 1 (c) were stirred with 80 ml of 2-methoxybenzylamine for 3.5 hours at 140° C. The almost colorless reaction solution which, had been cooled to about 80° C, was then diluted with 150 ml of ethanol, and the solution was introduced while stirring into 1.0 l of 1N hydrochloric acid at room temperature. The reaction product, which had precipitated in crystals, was suction-filtered and washed with water and then boiled up for a short time with 0.3 l of ethanol, during which the major part of it remained undissolved. After cooling to room temperature, it was suction-filtered and washed with ethanol and finally dried on a steam bath.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001284 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-b3c389bebe894e7c959fe5099f80df85 |
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| Source note | uspto-grants-1977_01 |
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