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Methanol → 2,4,4-Trimethyl-3-oxopentanenitrile

HRID 568592
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HRID 568592 반응식
[C:1]([O:7]C)(=O)[C:2]([CH3:5])([CH3:4])[CH3:3].[H-].[Na+].CO.[C:13](#[N:16])[CH2:14][CH3:15]>C1(C)C=CC=CC=1>[CH3:15][CH:14]([C:1](=[O:7])[C:2]([CH3:5])([CH3:4])[CH3:3])[C:13]#[N:16]
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참가 물질

6

반응물 4

HCID 887MethanolHCID 7854PropionitrileHCID 24758Sodium hydrideHCID 69027Methyl pivalate

생성물 1

HCID 1224002,4,4-Trimethyl-3-oxopentanenitrile

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

234.6 grams (2 moles) of methyl pivalate and 120 grams (2 moles) of sodium hydride (80 weight % suspension in white oil) were heated to 90° C. in 1500 ml of dry toluene. There were dropped in at this temperature after addition of 1 ml of methanol 233.3 grams (2 moles) of propionitrile within 2.5 hours. After the end of the development of hydrogen the suspension was extracted with a total of 1200 ml of water and after phase separation the aqueous phase was acidified with concentrated HCl to a pH of 2. The deposited oil was separated off, the water phase extracted with chloroform, the organic extracts combined, dried and concentrated. The residue was fractionated in a water jet vacuum. 2,4,4-trimethyl-3-oxopentanenitrile came over at 87° C./11 Torr in an amount of 226.1 grams (81.2% of theory).

후처리

  1. additionThere were dropped in at this temperature
  2. extractionAfter the end of the development of hydrogen the suspension was extracted with a total of 1200 ml of water
  3. customafter phase separation the aqueous phase
  4. customThe deposited oil was separated off
  5. extractionthe water phase extracted with chloroform
  6. customdried
  7. concentrationconcentrated
  8. customcame over at 87° C./11 Torr in an amount of 226.1 grams (81.2% of theory)

출처 및 근거

ORD 기록
ord-4b3cb3f6786e4e878a48942e22b393b5
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04728743

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