Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892317Generated: October 30, 2026

Hydrochloric Acid → N-(3-chlorophenyl)-1-(methylsulfonyl)-methanehydrazonoyl chloride

https://huagongshe.com/reaction/892317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-ChloroanilineHCID 7932—
ReactantSodium AcetateHCID 517045—
Reactant1-Chloro-1-methanesulfonyl-propan-2-oneHCID 22240418—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductN-(3-chlorophenyl)-1-(methylsulfonyl)-methanehydrazonoyl chlorideHCID 7387735281%

Reaction Conditions

Temperature0 °C

Reaction Steps

Part A. 3-Chloroaniline (5.00 g, 39.2 mmol) was added dropwise to an ice-cold 1N hydrochloric acid solution followed by the addition of 4 mL of 12M hydrochloric acid. To this solution was slowly added an ice-cold solution of sodium nitrite (3.00 g, 43.1 mmol) in 4 mL of water while maintaining the internal temperature to less than 5° C. This solution was stirred for 45 min at 0° C. during which time a precipitate formed. Glacial acetic acid (1 mL) was added and the precipitate dissolved. To this solution was added solid sodium acetate (approx. 2 g) to adjust the pH to 4 and then 10 mL ice cold acetone was added followed by an ice cold solution of 1-chloro-1-methanesulfonyl-propan-2-one in 10 mL acetone. The reaction was allowed to warm to ambient temperature and stirred for 14 h. A stream of nitrogen was passed over the solution to slightly reduce the solvent volume. The solid precipitate was collected by filtration, washed twice with water, and dried in vacuo at 40° C. to give 8.47 g (81%) of N-(3-chlorophenyl)-1-(methylsulfonyl)-methanehydrazonoyl chloride as a light orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005435B2
Source datasetuspto-grants-2006_02
ORD IDord-fce14e1b7ffc424e8888d2cd31167100
Source noteuspto-grants-2006_02