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Hydrochloric Acid → (+)-2-Fluoroheptyl p-toluenesulfonate

HRID 1449421
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1449421
[F:1][CH:2]([CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH2:3][OH:4].N1C=CC=CC=1.[C:16]1([CH3:26])[CH:21]=[CH:20][C:19]([S:22](Cl)(=[O:24])=[O:23])=[CH:18][CH:17]=1.Cl>>[C:16]1([CH3:26])[CH:21]=[CH:20][C:19]([S:22]([O:4][CH2:3][CH:2]([F:1])[CH2:5][CH2:6][CH2:7][CH2:8][CH3:9])(=[O:24])=[O:23])=[CH:18][CH:17]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 73974-Toluenesulfonyl chlorideHCID 15918973(-)-2-Fluoroheptanol

Produkt 1

HCID 14716844(+)-2-Fluoroheptyl p-toluenesulfonateAusbeute 66,7 %

Versuchsvorschrift

In a vessel sufficiently replaced with nitrogen, 0.40 g (3.0 mmol) of (-)-2-fluoroheptanol and 1.00 g (13 mmol) of dry pyridine were placed and dried for 30 min. under cooling on an ice bath. Into the solution, 0.69 g (3.6 mmol) of p-toluenesulfonyl chloride was added, and the mixture was stirred for 5 hours. After the reaction, 10 ml of 1N-HCl was added, and the resultant mixture was subjected to two times of extraction with 10 ml of methylene chloride. The extract liquid was washed once with 10 ml of distilled water and dried with an appropriate amount of anhydrous sodium sulfate, followed by distilling-off of the solvent to obtain 0.59 g (2.0 mmol) of (+)-2-fluoroheptyl p-toluenesulfonate.

Aufarbeitung

  1. customdried for 30 min.
  2. temperatureunder cooling on an ice bath
  3. additionwas added
  4. extractionthe resultant mixture was subjected to two times of extraction with 10 ml of methylene chloride
  5. washThe extract liquid was washed once with 10 ml of distilled water
  6. dry with materialdried with an appropriate amount of anhydrous sodium sulfate

Quellen und Nachweise

ORD-Eintrag
ord-ff27c6403109456197cf5c11589e06b1
Quelldatensatz
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05599479

Notizen zur Reaktion

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