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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651759Generated: October 27, 2026

Phosphate → Ethanol, 2-[(3-aminophenyl)sulfonyl]-

https://huagongshe.com/reaction/1651759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantBenzenesulfinic acid, 2-chloro-5-nitro-, sodium salt (1:1)HCID 111522—
Reactant2-(4-Chloro-3-nitrobenzenesulfonyl)ethanolHCID 13685284—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
ProductEthanol, 2-[(3-aminophenyl)sulfonyl]-HCID 78905—

Reaction Conditions

Temperature85 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929757
Source datasetuspto-grants-1990_05
ORD IDord-07ba1c764abe422a92c08e92bb4b62df
Source noteuspto-grants-1990_05