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Sodium Hydroxide → HCID 20324621, 화합물

HRID 436847
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HRID 436847 반응식
[CH2:1]([C:4]([NH2:10])([CH2:7][CH2:8][CH3:9])[C:5]#[CH:6])[CH2:2][CH3:3].Br[CH2:12][CH:13]=[O:14].[OH-].[Na+]>CO>[CH2:1]([C:4]([NH:10][CH2:12][CH:13]=[O:14])([CH2:7][CH2:8][CH3:9])[C:5]#[CH:6])[CH2:2][CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 105131Acetaldehyde, bromo-HCID 3046207HCID 3046207, 화합물

생성물 1

HCID 20324621HCID 20324621, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1,1-Dipropylprop-2-ynylamine (1.6 mole), the diethyl acetal of 2-bromoacetaldehyde (1.0 mole) and methanol (100 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is heated at reflux with stirring for a period of about 6 hours. After this time the reaction mixture is cooled to room temperature and sodium hydroxide (20 grams) is added. The reaction mixture is then stirred for an additional period of about 16 hours. The mixture is then filtered and the filtrate is distilled to yield the desired product the diethyl acetal of 2-(1,1-dipropylprop-2-ynylamino)acetaldehyde.

후처리

  1. customequipped with a mechanical stirrer
  2. temperaturethermometer and reflux condenser
  3. temperatureThe reaction mixture is heated
  4. temperatureat reflux
  5. stirringThe reaction mixture is then stirred for an additional period of about 16 hours
  6. filtrationThe mixture is then filtered
  7. distillationthe filtrate is distilled

출처 및 근거

ORD 기록
ord-6598859c54924dfeba380f1a3699c736
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04028375

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