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Triethylamine → HCID 10892715, Verbindung

HRID 2050489
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2050489
[Br:1][C@@H:2]([CH2:5][CH2:6][OH:7])[CH2:3][OH:4].C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17]>C(Cl)Cl>[Br:1][C@@H:2]([CH2:5][CH2:6][O:7][S:16]([CH3:15])(=[O:18])=[O:17])[CH2:3][O:4][S:16]([CH3:15])(=[O:18])=[O:17]
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Komponenten

5

Edukt 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 11095044(S)-2-Bromobutane-1,4-diol

Produkt 1

HCID 10892715HCID 10892715, VerbindungAusbeute 97 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A solution of 70 g (0.414 mol) (S)-2-bromo-1,4-butanediol in 1.5 liters methylene chloride was cooled in ice and 173 ml (1.24 mol) triethylamine (dried over potassium hydroxide) was added to give a clear solution. To this was added dropwise over 80 minutes at 5° to 15° C., 96 ml (1.24 mol) methanesulfonyl chloride. The mixture was then stirred at room temperature for 2.5 hours, washed 2×750 ml with water and 1×750 ml brine, dried (MgSO4), and the solvent evaporated to give an amber oil which was purified by chromatography on a 140 mm×25 cm silica gel column, eluting with 9:1 chloroform:ethyl acetate. The product fractions were combined and solvent evaporated to give 105 g (97%) of the title compound as a waxy white solid; [alpha]D =-34.49° (c=5 in CHCl3).

Aufarbeitung

  1. customto give a clear solution
  2. additionTo this was added dropwise over 80 minutes at 5° to 15° C.
  3. washwashed 2×750 ml with water and 1×750 ml brine
  4. dry with materialdried (MgSO4)
  5. customthe solvent evaporated
  6. customto give an amber oil which
  7. customwas purified by chromatography on a 140 mm×25 cm silica gel column
  8. washeluting with 9:1 chloroform
  9. customsolvent evaporated

Quellen und Nachweise

ORD-Eintrag
ord-134c7b1e45f74c8e8f2ef389cc49d9e5
Quelldatensatz
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05013729

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