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

Temperatur

0 °C

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.

1. temperaturewhile maintaining the internal temperature to less than 5° C
2. customformed
3. dissolutionthe precipitate dissolved
4. temperatureto warm to ambient temperature
5. stirringstirred for 14 h
6. filtrationThe solid precipitate was collected by filtration
7. washwashed twice with water
8. customdried in vacuo at 40° C.

ORD-Eintrag

ord-0a81cb324f0c436ba0fea4a281fefa71

Quelldatensatz

uspto-grants-2008_03

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07338963B2