Phenyl cyanate → 4-Dibutylamino-2-butynenitrile
Reaction equation
[Li][CH2:2][CH2:3][CH2:4][CH3:5].[CH2:6]([N:10]([CH2:14][CH2:15][CH2:16][CH3:17])CC#C)[CH2:7][CH2:8][CH3:9].C1(OC#[N:26])C=CC=CC=1>CCOCC>[CH2:2]([N:10]([CH2:14][CH2:15][CH2:16][CH3:17])[CH2:6][C:7]#[C:8][C:9]#[N:26])[CH2:3][CH2:4][CH3:5]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -70 °C
Procedure
n-BuLi (2.2 M, 69.5 mL, 0.153 mol) was added dropwise to a cooled (-78° C.) solution of 3-dibutylaminopropyne (24.9 g, 0.149 mol) in anhydrous ether (175 mL) at a rate not allowing the temperature to rise above -50° C. The resulting solution was stirred (5minutes, -70° C.), then phenyl cyanate (19.6 g, 0.164 mol) was added dropwise at a rate not allowing the temperature to rise above -60° C. The resulting solution was stirred (45 minutes, -78° C.), then warmed (25° C.). The resulting dark brown solution was diluted with ether (250 mL), washed with 3.0 N NaOH (3×170 mL), washed with brine (1×170 mL), then dried (MgSO4), and concentrated in vacuo. The resulting oil was chromatographed on silica (chloroform) to yield 27.0 g (94.4%) of 4-dibutylamino-2-butynenitrile as a brown liquid. 1H NMR (250 MHz, CDCl3): δ 3.53 (s, 2H), 2.46 (t, 4H), 1.36 (m, 8H), 0.92 (t, 6H).
Workup
- customto rise above -50° C
- customto rise above -60° C
- stirringThe resulting solution was stirred (45 minutes, -78° C.)
- temperaturewarmed (25° C.)
- washwashed with 3.0 N NaOH (3×170 mL)
- washwashed with brine (1×170 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- customThe resulting oil was chromatographed on silica (chloroform)
Sources & evidence
- ORD record
- ord-961b8d7a8ae34fa3a1d256a748f858d8
- Source dataset
- uspto-grants-1992_11
- Patent number
- US05162360
Reaction notes
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