Triethylamine → 2-Cyano-2-(2,4-dichlorophenyl)decyl methane sulfonate

HRID 616389Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 616389
[C:1]([C:3]([C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:15]=1[Cl:21])([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])[CH2:4][OH:5])#[N:2].[CH3:22][S:23](Cl)(=[O:25])=[O:24].C(N(CC)CC)C>C1C=CC=CC=1>[CH3:22][S:23]([O:5][CH2:4][C:3]([C:1]#[N:2])([C:14]1[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][C:15]=1[Cl:21])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13])(=[O:25])=[O:24]

Komponenten

5

Versuchsvorschrift

To a mixture of 2-cyano-2-(2,4-dichlorophenyl)decan-1-ol (40g., 0.12 mole) and methane sulfonyl chloride (15.3g., 0.13 mole) in 2 liters of benzene is added dropwise at 10° C., 14.8g., (0.14 mole) of triethylamine. The reaction mixture is stirred at room temperature for 30 minutes and then heated on a steam bath for another 30 minutes. The precipitate formed is filtered and the filtrate is washed with dilute hydrochloric acid, water, saturated sodium bicarbonate solution, saturated sodium chloride solution and dried over magnesium sulfate. The solvent is evaporated to give 41.3g. of product, which is identified by nmr.

Aufarbeitung

  1. additionis added dropwise at 10° C.
  2. temperatureheated on a steam bath for another 30 minutes
  3. customThe precipitate formed
  4. filtrationis filtered
  5. washthe filtrate is washed with dilute hydrochloric acid, water, saturated sodium bicarbonate solution, saturated sodium chloride solution
  6. dry with materialdried over magnesium sulfate
  7. customThe solvent is evaporated
  8. customto give 41.3g

Quellen und Nachweise

ORD-Eintrag
ord-bd779e6425a449329db0520239f4d541
Quelldatensatz
uspto-grants-1978_02
Patentnummer
US04073921

Notizen zur Reaktion

Wird geladen…