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Phenyl isocyanate → 5-Isoxazolemethanol, 3-dodecyl-

HRID 375958
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 375958
[N+:1]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])([O-:3])=O.C[Si](C)(C)[O:19][C:20]#[C:21][CH3:22].C1(N=C=O)C=CC=CC=1.C(N(CC)CC)C>C1C=CC=CC=1>[CH2:5]([C:4]1[CH:22]=[C:21]([CH2:20][OH:19])[O:3][N:1]=1)[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 7672Phenyl isocyanateHCID 8471TriethylamineHCID 108233151-NitrotridecaneHCID 13614841O-trimethylsilylpropynol

Produkt 1

HCID 106355535-Isoxazolemethanol, 3-dodecyl-Ausbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 241
Benzene
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of 1-nitrotridecane (10.5 g) and O-trimethylsilyl-propynol (5.88 g) in dry benzene (100 ml) was added dropwise a solution of freshly distilled phenylisocyanate (10.9 g) and triethylamine (5.56 g) in dry benzene (40 ml) at 40° C., with mechanical stirring. The mixture was heated to 60° C. for 3.5 hr, cooled, and filtered. The filtrate was evaporated, taken up in tetrahydrofuran (300 ml) and 1.0M tetrabutylammonium fluoride (8 ml) was added. After 30 mins, the mixture was evaporated and the residue was purified by flash chromatography (silica gel, 2% methanol:dichloromethane). The appropriate fractions were collected and evaporated to give 10.5 g (86%) of product, mp 61°-63° C.

Aufarbeitung

  1. temperaturecooled
  2. filtrationfiltered
  3. customThe filtrate was evaporated
  4. addition1.0M tetrabutylammonium fluoride (8 ml) was added
  5. customthe mixture was evaporated
  6. customthe residue was purified by flash chromatography (silica gel, 2% methanol:dichloromethane)
  7. customThe appropriate fractions were collected
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-b34b50964c6047ada276ceb46827389e
Quelldatensatz
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05488063

Notizen zur Reaktion

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