Chlorosulfonic acid → 5,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-2-naphthalenesulfonyl chloride

HRID 1599113

Reaktionsgleichung

Reaktionsgleichung von HRID 1599113
[CH3:1][C:2]1([CH3:14])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([CH3:13])([CH3:12])[CH2:4][CH2:3]1.[Cl:15][S:16](O)(=[O:18])=[O:17]>>[CH3:1][C:2]1([CH3:14])[CH2:3][CH2:4][C:5]([CH3:13])([CH3:12])[C:6]2[CH:7]=[C:8]([S:16]([Cl:15])(=[O:18])=[O:17])[CH:9]=[CH:10][C:11]1=2

Komponenten

3

Edukt 2

HCID 24638Chlorosulfonic acidHCID 811861,1,4,4-Tetramethyltetralin

Produkt 1

HCID 27954675,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-2-naphthalenesulfonyl chloride

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

94.0 g (0.5 mol) of 1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene were stirred into 100 ml of chlorosulfonic acid at 20° C. within 30 min. The reaction solution was maintained at 60° C. for 1 hour, cooled to room temperature and then poured into 1.5 1 of ice and extracted with ether. The organic phase was washed to neutrality with brine and water, dried over magnesium sulfate and evaporated under reduced pressure. Recrystallization of the residue from methanol yielded 55.0 g of 5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene-2-sulfonyl chloride of melting point 71°-74° C.

Aufarbeitung

  1. temperaturecooled to room temperature
  2. additionpoured into 1.5 1 of ice
  3. extractionextracted with ether
  4. washThe organic phase was washed
  5. dry with materialdried over magnesium sulfate
  6. customevaporated under reduced pressure
  7. customRecrystallization of the residue from methanol

Quellen und Nachweise

ORD-Eintrag
ord-8ca6d8b73c0d436d8f0f8b7f0ab5a3b3
Quelldatensatz
uspto-grants-1998_04
Patentnummer
US05739374

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