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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287784Generated: October 31, 2026

HCID 21506073, compound → HCID 21506108, compound

https://huagongshe.com/reaction/1287784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21506073HCID 21506073—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 21506108HCID 21506108—

Reaction Steps

A solution of ethyl-3-allylamino-4-phenoxy-5-sulphamyl-benzoate (1.65 g) in ethanol (150 ml) was hydrogenated at room temperature and 1.1. atmospheres hydrogen pressure after the addition of a palladium-on-carbon catalyst (0.6 g catalyst containing 10% Pd). After the hydrogen uptake had become negligible, the catalyst was removed by filtration, and the filtrate was evaporated in vacuo. The residue was recrystallized twice from aqueous ethanol, resulting in ethyl-4-phenoxy-3-n-propylamino-5-sulphamyl-benzoate with a melting point of 150°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985777
Source datasetuspto-grants-1976_10
ORD IDord-687e16c009634ee5af15efb7c3e6af54
Source noteuspto-grants-1976_10