Sodium Hydroxide → 3-Cyclopentylpropiolonitrile

HRID 44932

반응식

HRID 44932 반응식
[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

참가 물질

7

반응물 4

HCID 14798Sodium HydroxideHCID 70740Phenyl cyanateHCID 136725CyclopentylacetyleneHCID 178418339Butyllithium

생성물 1

HCID 574776163-Cyclopentylpropiolonitrile수율 95%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회HCID 8058Hexane용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-d4fd9454a0bc4abebbd8517846720ea5
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08541425B2

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