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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834757Generated: October 31, 2026

Sodium Hydroxide → HCID 19819855, compound

https://huagongshe.com/reaction/1834757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfiteHCID 24437—
ReactantN-[4-(Butane-1-sulfonyl)phenyl]ethanimidic acidHCID 237535—
ReactantSodium NitriteHCID 23668193—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 19819855HCID 1981985570%

Reaction Conditions

Temperature0 °C

Reaction Steps

255 g of p-butylsulphonylacetanilide, in a mixture of 1.5 l of water and 300 ml of concentrated hydrochloric acid, are boiled for 1 hour under reflux. After cooling to 0° C, the product is diazotised with a solution of 70 g of NaNO2 in 175 ml of water. The filtered diazonium salt solution is added, at 5°-10° C, to a mixture of 750 g of 40% strength sodium sulphite solution and 750 ml of water which had been adjusted to pH 7 with concentrated sodium hydroxide solution, the pH being maintained at 6-7 by means of concentrated sodium hydroxide solution. After standing overnight, 300 ml of concentrated hydrochloric acid are added and the mixture is boiled for 1 hour. p-Butylsulphonylphenylhydrazine of melting point 138° C (from ethanol) is obtained, in a yield of approx. 70- 75% of theory, from the cooled solution by careful addition of alkali.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04071466
Source datasetuspto-grants-1978_01
ORD IDord-abc88074ae2f4e0bbd6cbe2d758bc98c
Source noteuspto-grants-1978_01