Water → Methyl-(8-phenyl-1,4-dioxaspiro[4.5]dec-8-yl)amine

HRID 1948591Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1948591
[H-].[H-].[H-].[H-].[Li+].[Al+3].[N:7]([C:10]1([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH2:19][CH2:18][C:13]2([O:17][CH2:16][CH2:15][O:14]2)[CH2:12][CH2:11]1)=[C:8]=O.[OH-].[Na+].O>C1COCC1>[CH3:8][NH:7][C:10]1([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH2:11][CH2:12][C:13]2([O:17][CH2:16][CH2:15][O:14]2)[CH2:18][CH2:19]1

Komponenten

6

Versuchsvorschrift

LiAlH4 (535 mg, 14.08 mmole) was suspended in dry THF (4 ml) with the exclusion of atmospheric moisture. 8-isocyanato-8-phenyl-1,4-dioxaspiro[4.5]decane (2.29 g, 8.8 mmole, dissolved in 40 ml of dry THF) was then added dropwise within 20 minutes. After the end of the addition the reaction mixture was boiled under reflux for 4 hours. After cooling the reaction mixture, aqueous THF (1 ml H2O in 3 ml) was first of all carefully added, followed by 1.7 ml of 15% sodium hydroxide solution and finally 5 ml of H2O. The reaction mixture was stirred for 20 minutes and then filtered through diatomaceous earth. The solvent mixture obtained by washing the filter cake several times with ethyl acetate was concentrated by evaporation to dryness on a rotary evaporator. The desired product was obtained in a yield of 2.1 g (97%) as a viscous oil.

Aufarbeitung

  1. additionAfter the end of the addition the reaction mixture
  2. temperatureunder reflux for 4 hours
  3. additionall carefully added
  4. filtrationfiltered through diatomaceous earth
  5. customThe solvent mixture obtained
  6. washby washing the filter cake several times with ethyl acetate
  7. concentrationwas concentrated by evaporation to dryness on a rotary evaporator

Quellen und Nachweise

ORD-Eintrag
ord-cadcc3530cbc4494ada6956d419cc7c4
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08399503B2

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