2,2-Diethylmalononitrile → 1,3-Diamino-2,2-diethylpropane

HRID 1024337노트

반응식

HRID 1024337 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH2:7]([C:9]([CH2:14][CH3:15])([C:12]#[N:13])[C:10]#[N:11])[CH3:8]>CCOCC>[CH2:7]([C:9]([CH2:14][CH3:15])([CH2:12][NH2:13])[CH2:10][NH2:11])[CH3:8]

참가 물질

4

반응물 2

HCID 27772312,2-DiethylmalononitrileHCID 21226445Aluminium lithium hydride

생성물 1

HCID 4325891,3-Diamino-2,2-diethylpropane

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

A suspension of LiAlH4 (4.66 g) in dry Et2O (100 mL) was cooled in an ice bath, and a solution of 2,2-diethyl-malononitrile (5.0 g) in Et2O (50 mL) was added dropwise at such a rate that the temperature was kept below 20° C. The mixture was stirred overnight at room temperature, cooled in an ice bath, and quenched by adding H2O (5 mL), 2M aqueous NaOH (10 mL) and again H2O (5 mL). The suspension was filtered, the filter cake was washed with Et2O, and the combined filtrates were evaporated to dryness under reduced pressure to give 5.0 g of a clear, light-yellow liquid. 1H NMR (400 MHz, CDCl3) δ 0.80 (t, J=8 Hz, 6H), 1.08 (br s, 4H), 1.22 (q, J=8 Hz, 4H), 2.52 (s, 4H).

후처리

  1. temperaturewas cooled in an ice bath
  2. customwas kept below 20° C
  3. temperaturecooled in an ice bath
  4. customquenched
  5. additionby adding H2O (5 mL), 2M aqueous NaOH (10 mL) and again H2O (5 mL)
  6. filtrationThe suspension was filtered
  7. washthe filter cake was washed with Et2O
  8. customthe combined filtrates were evaporated to dryness under reduced pressure
  9. customto give 5.0 g of a clear, light-yellow liquid

출처 및 근거

ORD 기록
ord-2b4ed2c08f70401892cf94dae688719d
출처 데이터셋
uspto-grants-2014_05
특허 번호
US08722887B2

반응 노트

불러오는 중…