Triethylamine → HCID 21802382, Verbindung

HRID 1656017Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1656017
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([NH:19][CH:20]=O)([CH2:15][CH2:16][CH2:17][CH3:18])[CH2:9][N:10]2[CH:14]=[N:13][CH:12]=[N:11]2)=[CH:4][CH:3]=1.C(N(CC)CC)C.F[B-](F)(F)F.C([N+]1C2C=CC=CC=2OC=1Cl)C>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([N+:19]#[C-:20])([CH2:15][CH2:16][CH2:17][CH3:18])[CH2:9][N:10]2[CH:14]=[N:13][CH:12]=[N:11]2)=[CH:4][CH:3]=1

Komponenten

5

Versuchsvorschrift

To a stirred solution of 0.40 g (1.3 mmols) of N-[2-(4-chlorophenyl)-1-(1,2,4-triazol-1-yl)-2-hexyl]formamide in 5 mL of methylene chloride under nitrogen was added 0.45 mL (3.26 mmols) of triethylamine. To this mixture was added a slurry of 0.439 g (1.63 mmols) of 3-ethyl-2-chlorobenzoxazolium tetrafluoroborate, which was weighed out under a nitrogen atmosphere, in 5 mL of methylene chloride. The reaction mixture was then allowed to stir at room temperature for 12 hours. The reaction mixture was poured into ice water and extracted with ethyl acetate. The combined organic layers were washed once with 10% hydrochloric acid, brine, and dried over magnesium sulfate. Removal of solvents gave a crude oil which was purified by column chromatography (Merck 60 silica gel, ethyl acetate/hexane) to give 0.20 g (52%) of a clear, colorless oil.

Aufarbeitung

  1. extractionextracted with ethyl acetate
  2. washThe combined organic layers were washed once with 10% hydrochloric acid, brine
  3. dry with materialdried over magnesium sulfate
  4. customRemoval of solvents
  5. customgave a crude oil which
  6. customwas purified by column chromatography (Merck 60 silica gel, ethyl acetate/hexane)
  7. customto give 0.20 g (52%) of a clear, colorless oil

Quellen und Nachweise

ORD-Eintrag
ord-e4719c960f974106af2b92994f759c02
Quelldatensatz
uspto-grants-1993_10
Patentnummer
US05252594

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