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Hydrochloric Acid → HCID 178509126, 화합물

HRID 616435
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HRID 616435 반응식
[N:1]1([CH2:7][C:8](=[CH2:11])[C:9]#[N:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:12]1([NH:18][NH2:19])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[O-]CC.[Na+].Cl>C(O)C>[N:1]1([CH2:7][CH:8]2[CH2:11][N:18]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)[NH:19][C:9]2=[NH:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 7516PhenylhydrazineHCID 2723922Sodium ethoxideHCID 27768462-(Piperidin-1-ylmethyl)prop-2-enenitrile

생성물 1

HCID 178509126HCID 178509126, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

α-Piperidinomethylacrylonitrile (17g) and phenylhydrazine (10.8g) were added to a solution of sodium ethoxide (2.3g sodium) in ethanol (200 ml). The resulting solution was boiled under reflux for 2 hours and a solid precipitate formed during the reaction. Dilute hydrochloric acid (50 ml of 2N) was added to the reaction mixture and the solution was evaporated to dryness. The solid residue was extracted with dry ethanol and the product crystallised from the ethanol as colourless plates (melting point 186-7° C).

후처리

  1. temperatureunder reflux for 2 hours
  2. customa solid precipitate formed during the reaction
  3. customthe solution was evaporated to dryness
  4. extractionThe solid residue was extracted with dry ethanol
  5. customthe product crystallised from the ethanol as colourless plates (melting point 186-7° C)

출처 및 근거

ORD 기록
ord-9509c18841724e1bb4d07628c541990a
출처 데이터셋
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04074051

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