HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654378Generated: October 27, 2026
Benzenesulfonyl chloride → 2-Hydroxy-3-ethoxybenzaldehyde benzenesulphonate
https://huagongshe.com/reaction/654378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | O-Ethylvanillin | HCID 68117 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxy-3-ethoxybenzaldehyde benzenesulphonate | HCID 88444822 | 98% |
Reaction Steps
3-Ethoxysalicylaldehyde (498 g, 3 moles) and sodium hydroxide (140 g, 3.5 moles) in 1.5 liters of water are introduced into a 4 liter reactor provided with mechanical stirring, a condenser and a nitrogen inlet. The mixture is taken to 60° C. and benzenesulphonyl chloride is added dropwise over three-quarters of an hour. The mixture is heated to 75° C. for a quarter of an hour. It is cooled. An oil forms which crystallizes with time. It is filtered, washed with water and dried. The 2-hydroxy-3-ethoxybenzaldehyde benzenesulphonate (901 g, yield=98%) is used for the following stage. It can be recrystallized from 90:10 acetic acid/water. A white powder is obtained, m.p.=68°-69° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05131911 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-2c8013f923a7457588161d646a65a30d |
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| Source note | uspto-grants-1992_07 |
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