Sodium Chloride → 2,4-Hexadiyn-1,6-diol bis(p-methoxybenzene sulfonate)

HRID 903545

Reaktionsgleichung

Reaktionsgleichung von HRID 903545
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9](Cl)(=[O:11])=[O:10])=[CH:5][CH:4]=1.[CH2:13]([OH:20])[C:14]#[C:15][C:16]#[C:17][CH2:18][OH:19].[OH-:21].[K+].[Cl-].[Na+]>O1CCCC1.O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([O:19][CH2:18][C:17]#[C:16][C:15]#[C:14][CH2:13][O:20][S:9]([C:6]2[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)(=[O:10])=[O:21])(=[O:11])=[O:10])=[CH:5][CH:4]=1

Komponenten

7

Versuchsvorschrift

Fifty grams of p-methoxybenzenesulfonyl chloride was reacted, at 15° to 18° C., with 11 grams of 2,4-hexadiyn-1,6-diol in 100 ml tetrahydrofuran, while a solution of 20 grams potassium hydroxide in 180 ml water was added dropwise over a 10 minute period. The resulting exothermic reaction was cooled at 15° to 18° C. with the aid of an ice-water bath. After the addition of the potassium hydroxide solution, the solution was allowed to stir overnight at room temperature. The mixture was then poured into 500 ml cold aqueous sodium chloride solution which resulted in a yellow precipitate. The precipitate was collected by filtration, washed with water and dried. Obtained was 41.6 grams (93% yield of theory) of a yellow brown solid, melting point 120° to 122° C.

Aufarbeitung

  1. additionwas added dropwise over a 10 minute period
  2. customThe resulting exothermic reaction
  3. temperaturewas cooled at 15° to 18° C. with the aid of an ice-water bath
  4. customresulted in a yellow precipitate
  5. filtrationThe precipitate was collected by filtration
  6. washwashed with water
  7. customdried
  8. customObtained

Quellen und Nachweise

ORD-Eintrag
ord-e2e002cfcdfe4caa8f00335a0f59b455
Quelldatensatz
uspto-grants-1980_10
Patentnummer
US04228126

Verknüpfte Notizen

Wird geladen…