Piperidine → N-(2-chloroethyl)benzenesulfonamide

HRID 1834745Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1834745
O[CH2:2][CH2:3][NH:4][S:5]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)(=[O:7])=[O:6].N1CCCCC1.S(Cl)([Cl:23])(=O)=O>C(Cl)(Cl)(Cl)Cl>[Cl:23][CH2:2][CH2:3][NH:4][S:5]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)(=[O:7])=[O:6]

Komponenten

5

Edukt 3

HCID 8082PiperidineHCID 24648Sulfuryl chlorideHCID 1722145N-(2-hydroxyethyl)benzenesulfonamide

Produkt 1

HCID 4562550N-(2-chloroethyl)benzenesulfonamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 5943Carbon TetrachlorideKatalysator

Versuchsvorschrift

40.2 g. of N-(β-hydroxyethyl)-benzene sulfonamide was slurried in 100 ml. of carbon tetrachloride containing 5 drops of piperidine. Then, 47.6 g. of sulfonyl chloride was added over 10 minutes, keeping the temperature at 20°-25° C. during the addition. The reaction was completed by heating on a steam bath for one hour. The mixture was concentrated on the steam bath, dissolved in benzene and washed twice with dilute aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and the benzene evaporated on the steam bath with air. The product was crystallized from benzene cyclohexane to yield 28.0 g. of product, m.p. 58°-62° C.

Aufarbeitung

  1. customat 20°-25° C.
  2. additionduring the addition
  3. temperatureby heating on a steam bath for one hour
  4. concentrationThe mixture was concentrated on the steam bath
  5. dissolutiondissolved in benzene
  6. washwashed twice with dilute aqueous solution of sodium chloride
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. customthe benzene evaporated on the steam bath with air
  10. customThe product was crystallized from benzene cyclohexane
  11. customto yield 28.0 g

Quellen und Nachweise

ORD-Eintrag
ord-13de535d5daa4e4f81e5d991e962055f
Quelldatensatz
uspto-grants-1978_01
Patentnummer
US04071353

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