Sodium Hydroxide → 3-Cyclopentylpropiolonitrile

HRID 44932

Reaktionsgleichung

Reaktionsgleichung von HRID 44932
[CH:1]1([C:6]#[CH:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.C([Li])CCC.C1(O[C:20]#[N:21])C=CC=CC=1.[OH-].[Na+]>C1COCC1.CCCCCC>[CH:1]1([C:6]#[C:7][C:20]#[N:21])[CH2:5][CH2:4][CH2:3][CH2:2]1

Komponenten

7

Versuchsvorschrift

To a solution of cyclopentylacetylene (0.50 g, 5.3 mmol) in THF (5 mL) at −78° C. was added 2.5 M n-butyllithium in hexane (2.23 mL). The mixture was stirred for 15 min followed by the dropwise addition of phenyl cyanate (0.70 g, 5.8 mmol) in THF (3 mL). The reaction was warmed to room temperature. Into the reaction mixture was poured 6 N NaOH, and the mixture was stirred for 5 minutes. The product was extracted with diethyl ether. The extracts were washed with 6 N NaOH and with brine, then dried over sodium sulfate, decanted and the solvent was removed in vacuo to afford product (600 mg, 95%). 1H NMR (300 MHz, CDCl3): 2.81-2.68 (m, 1H), 2.07-1.54 (m, 8H).

Aufarbeitung

  1. stirringthe mixture was stirred for 5 minutes
  2. extractionThe product was extracted with diethyl ether
  3. washThe extracts were washed with 6 N NaOH and with brine
  4. dry with materialdried over sodium sulfate
  5. customdecanted
  6. customthe solvent was removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-d4fd9454a0bc4abebbd8517846720ea5
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08541425B2

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