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(R)-1-Phenylpropylamine → (R)-(+)-1-Phenylpropyl isocyanate

HRID 321936
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 321936
[C:1]1([C@H:7]([NH2:10])[CH2:8][CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.C[CH2:13][O:14]CC>CCOCC>[C:1]1([C@H:7]([N:10]=[C:13]=[O:14])[CH2:8][CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 5324978(R)-1-PhenylpropylamineHCID 10953452Ether hydrochloride

Produkt 1

HCID 7018288(R)-(+)-1-Phenylpropyl isocyanate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

To a solution of 1(R)-phenylpropylamine (14.33 g, 106 mmol) in Et2O (102 mL) was added a 1.0 M solution of HCl/Et2O (212 mL, 212 mmol). The mixture was stirred for 30 min, then the crude solution was evaporated to dryness on a rotary evaporator. The resulting white hydrochloride salt was suspended in toluene (200 mL), triphosgene was added (11.67 g, 39.3 mmol) and the resulting suspension was stirred at reflux for 3 h at room temperature overnight. The reaction mixture was concentrated and the final volume adjusted to 200 mL with toluene giving a final concentration of 0.53M. The resulting isocyanate solution was used as such. An aliquot (170 mL) was concentrated to give a colorless oil.

Aufarbeitung

  1. customthe crude solution was evaporated to dryness on a rotary evaporator
  2. additiontriphosgene was added (11.67 g, 39.3 mmol)
  3. stirringthe resulting suspension was stirred
  4. concentrationThe reaction mixture was concentrated
  5. concentrationAn aliquot (170 mL) was concentrated
  6. customto give a colorless oil

Quellen und Nachweise

ORD-Eintrag
ord-3d377779649647939bbbe6a1324bee03
Quelldatensatz
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06211170B1

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