Phenyl cyanate → 4-Cyclopentyl-but-2-ynenitrile

HRID 1353121

Reaction equation

HRID 1353121 reaction equation
[CH2:1]([CH:4]1[CH2:8][CH2:7][CH2:6][CH2:5]1)[C:2]#[CH:3].[Li]CCCC.C1(O[C:21]#[N:22])C=CC=CC=1>CCOCC>[CH:4]1([CH2:1][C:2]#[C:3][C:21]#[N:22])[CH2:8][CH2:7][CH2:6][CH2:5]1

Participants

5

Conditions

Temperature
-78 °C

Procedure

Prop-2-ynyl-cyclopentane (46.2 mmol) was dissolved in 100 mL of anhydrous Et2O under N2 and the reaction was cooled to −78° C. A 2.5 M solution of BuLi in hexanes (55.5 mmol) was added dropwise to the reaction over 30 minutes. The reaction was stirred for an additional 20 minutes and phenyl cyanate (55.5 mmol) was then added in solution with 20 mL of Et2O dropwise over 20 minutes. The resultant solution was allowed to slowly warm to rt and stir for 3 hours. The reaction material was then diluted in 200 mL of fresh Et2O and washed with three 100 mL portions of 1 N aqueous NaOH solution. The organics were then washed with 200 mL of brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified through flash chromatography on silica gel to give 4-cyclopentyl-but-2-ynenitrile (21.7 mmol).

Workup

  1. temperatureto slowly warm to rt
  2. stirringstir for 3 hours
  3. washwashed with three 100 mL portions of 1 N aqueous NaOH solution
  4. washThe organics were then washed with 200 mL of brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified through flash chromatography on silica gel

Sources & evidence

ORD record
ord-58662001d63c48e79d3be55517eee19b
Source dataset
uspto-grants-2007_05
Patent number
US07220865B2

Linked notes

Loading…