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llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
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Ethylamine → 2,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-

HRID 1464783
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1464783
C(N)C.Cl.NO.[CH2:7]([OH:10])[C:8]#[CH:9].Br[C:12]#[C:13][C:14]([O:17][CH3:18])([CH3:16])[CH3:15]>CO.[Cu]Cl>[CH3:18][O:17][C:14]([CH3:16])([CH3:15])[C:13]#[C:12][C:9]#[C:8][CH2:7][OH:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 6341EthylamineHCID 7859Propargyl alcoholHCID 443297Hydroxyamine hydrochlorideHCID 103522261-Butyne, 1-bromo-3-methoxy-3-methyl-

Produkt 1

HCID 99894232,4-Heptadiyn-1-ol, 6-methoxy-6-methyl-Ausbeute 89,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 62652
Cuprous chloride
Katalysator
HCID 887MethanolLösungsmittel2×

Versuchsvorschrift

200 ml of a 70% aqueous solution of ethyamine, 1 g of copper(I) chloride, 5 g of hydroxylamine hydrochloride and 25 g of propargyl alcohol were dissolved in 500 ml of methanol, and with ice cooling and stirring, a methanol solution (100 ml) of 74 g of 1-bromo-3-methoxy-3-methyl-1-butyne was added. The mixture was stirred at room temperature for 1 hour, and then the solvent was evaporated. Water and ethyl acetate were added, and the insoluble material was removed by filtration. The organic layer separated was worked up in a customary manner, and the product was purified by vacuum distillation ( b.p. -97° C. / 2 mmHg ) to give 57 g of the captioned compound as a colorless oil.

Aufarbeitung

  1. stirringThe mixture was stirred at room temperature for 1 hour
  2. customthe solvent was evaporated
  3. additionWater and ethyl acetate were added
  4. customthe insoluble material was removed by filtration
  5. customThe organic layer separated
  6. distillationthe product was purified by vacuum distillation ( b.p. -97° C. / 2 mmHg )

Quellen und Nachweise

ORD-Eintrag
ord-1a16649ea5e848ea93612e0392f12700
Quelldatensatz
uspto-grants-1994_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05306728

Notizen zur Reaktion

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