HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651759Generated: October 27, 2026
Phosphate → Ethanol, 2-[(3-aminophenyl)sulfonyl]-
https://huagongshe.com/reaction/1651759
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphate | HCID 1061 | — |
| Reactant | Benzenesulfinic acid, 2-chloro-5-nitro-, sodium salt (1:1) | HCID 111522 | — |
| Reactant | 2-(4-Chloro-3-nitrobenzenesulfonyl)ethanol | HCID 13685284 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethanol, 2-[(3-aminophenyl)sulfonyl]- | HCID 78905 | — |
Reaction Steps
102.6 g of moist paste of 2-chloro-5-nitrophenyl 2-hydroxyethyl sulphone from Example 1 [or an equimolar amount of 4-chloro-3-nitrophenyl 2-hydoxyethyl sulphone] are stirred into 250 ml of water and 50 ml of the phosphate buffer solution described under Example 2. A small amount of a nonionic emulsifier and 5 g of palladium-oncharcoal catalyst are added. Hydrogenation with hydrogen is then carried out in an autoclave at 70° C. and approximately 40 bar. The reduction is monitored by chromatography. After the hydrogenation, and after releasing the pressure and flushing the reactor, the product is heated to 85° C. and clarified via a pressure filter. The filter is cooled to 0° C. and the crystalline 3-aminophenyl 2-hydroxyethyl sulphone is isolated by filtration. 53 g of single-substance product are obtained after drying.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04929757 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-07ba1c764abe422a92c08e92bb4b62df |
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| Source note | uspto-grants-1990_05 |
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