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Ammonium Hydroxide → 5-Chloropentanesulfonamide

HRID 2396694
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2396694
[OH-].[NH4+:2].[Cl:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][S:9](Cl)(=[O:11])=[O:10]>O1CCCC1>[Cl:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][S:9]([NH2:2])(=[O:11])=[O:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14923Ammonium HydroxideHCID 12589202HCID 12589202, Verbindung

Produkt 1

HCID 99899625-Chloropentanesulfonamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

2.5 ml of a 28% aqueous solution of ammonium hydroxide were added dropwise at 0° to +5° C. under an inert gas atmosphere to a solution of 2.5 g of 5-chloropentane sulfonyl chloride (preparation described in: Bull. Soc. Chim. Belg. (1965) Vol. 74., p. 21) in 30 ml of tetrahydrofuran. The temperature was allowed to rise from 3° C. to 16° C., and the mixture was stirred at ambient temperature for 2 hours. The tetrahydrofuran was evaporated under reduced pressure and the residue was taken up in water, extracted with methylene chloride, washed with water, then with an aqueous solution of sodium chloride, dried and evaporated under reduced pressure to obtain 2.01 g of the expected product melting at 62° C.

Aufarbeitung

  1. customto rise from 3° C. to 16° C.
  2. customThe tetrahydrofuran was evaporated under reduced pressure
  3. extractionextracted with methylene chloride
  4. washwashed with water
  5. dry with materialwith an aqueous solution of sodium chloride, dried
  6. customevaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-c163d5683b9a4217b9fdabfcd2b0a7a9
Quelldatensatz
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05494907

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