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Acetic Anhydride → 1-Acetyl-6-hydroxymethyl-1,2,3,4-tetrahydroquinoline

HRID 636520
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 636520
[OH:1][CH2:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[NH:9][CH2:8][CH2:7][CH2:6]2.[C:13](OC(=O)C)(=[O:15])[CH3:14]>CO>[C:13]([N:9]1[C:10]2[C:5](=[CH:4][C:3]([CH2:2][OH:1])=[CH:12][CH:11]=2)[CH2:6][CH2:7][CH2:8]1)(=[O:15])[CH3:14]
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Komponenten

4

Edukt 2

HCID 7918Acetic AnhydrideHCID 226628871,2,3,4-Tetrahydroquinolin-6-ylmethanol

Produkt 1

HCID 212548181-Acetyl-6-hydroxymethyl-1,2,3,4-tetrahydroquinolineAusbeute 57,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of 6-hydroxymethyl-1,2,3,4-tetrahydroquinoline (314 mg) in methanol (4 ml) was dropwise added acetic anhydride (589 mg) under ice-cooling, and the mixture was stirred for 1 hour at the same temperature. The solvent was removed in vacuo, and ethyl acetate and saturated sodium bicarbonate solution were added to the residue. The organic layer was washed with water and brine, dried and concentrated in vacuo. The residue was purified by preparative thin-layer chromatography (n-hexane:ethyl acetate=1:2, v/v) to give 1-acetyl-6-hydroxymethyl-1,2,3,4-tetrahydroquinoline (227 mg).

Aufarbeitung

  1. temperaturecooling
  2. customThe solvent was removed in vacuo, and ethyl acetate and saturated sodium bicarbonate solution
  3. additionwere added to the residue
  4. washThe organic layer was washed with water and brine
  5. customdried
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by preparative thin-layer chromatography (n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-0eaf76970b8e4595baf88e6ff442a0fc
Quelldatensatz
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06194396B1

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