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Sodium hydride → HCID 178420294, Verbindung

HRID 1898888
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1898888
[H-].[Na+].[C:3]1([C@@H:9]2[CH2:14][CH2:13][C@H:12]([OH:15])[CH2:11][CH2:10]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Cl[C:17]1[C:26]2[CH2:25][CH2:24][CH2:23][CH2:22][C:21]=2[N:20]=[CH:19][N:18]=1.[NH4+].[Cl-]>C1COCC1>[C:3]1([C@@H:9]2[CH2:10][CH2:11][C@H:12]([O:15][C:17]3[C:26]4[CH2:25][CH2:24][CH2:23][CH2:22][C:21]=4[N:20]=[CH:19][N:18]=3)[CH2:13][CH2:14]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 125829694-Chloro-5,6,7,8-tetrahydroquinazolineHCID 178521547HCID 178521547, Verbindung

Produkt 1

HCID 178420294HCID 178420294, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028
Tetrahydrofuran
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

0.5 g (16.7 mmol) of 80% NaH was added in portions to a solution of 1.85 g (105 mmol) of cis-4-phenylcyclohexanol in 30 ml of absolute THF. After this, the mixture was heated for 1 hour at 50° C., and 1.5 g (8.75 mmol) of 4-chloro-5,6,7,8-tetrahydroquinazoline, dissolved in 15 ml of absolute THF, were added dropwise. The reaction mixture was subsequently refluxed for 2 hours. After the mixture had cooled to room temperature, it was poured into saturated NH4Cl solution and this was extracted with ether, and the combined organic phase was dried over MgSO4. The solvent was evaporated in vacuo, and the residue (2.7 g) was purified by flash chromatography over silica gel, using n-hexane/ethyl acetate (2:1). Concentration gave 1.5 g (50.2% of theory), colorless crystals, m.p. 109° C. ##STR12##

Aufarbeitung

  1. additionwere added dropwise
  2. temperatureThe reaction mixture was subsequently refluxed for 2 hours
  3. temperatureAfter the mixture had cooled to room temperature
  4. extractionthis was extracted with ether
  5. dry with materialthe combined organic phase was dried over MgSO4
  6. customThe solvent was evaporated in vacuo
  7. customthe residue (2.7 g) was purified by flash chromatography over silica gel
  8. concentrationConcentration
  9. customgave 1.5 g (50.2% of theory), colorless crystals, m.p. 109° C.

Quellen und Nachweise

ORD-Eintrag
ord-03d1dba484164f70a713fba3ca4b65b4
Quelldatensatz
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05571815

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