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Formaldehyde → HCID 86704561, 화합물

HRID 1022432
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HRID 1022432 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:11])[C:9]#[N:10])=[CH:4][CH:3]=1.[CH2:12]=[O:13]>N1C=CC=CC=1.CO.O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([CH3:11])([CH2:12][OH:13])[C:9]#[N:10])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 712FormaldehydeHCID 107509272-(4-Bromophenyl)propanenitrile

생성물 1

HCID 86704561HCID 86704561, 화합물수율 84%

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매HCID 1049Pyridine용매

실험 절차

To a stirred solution of 2-(4-bromo-phenyl)-propionitrile (27 g, 128.5 mmol) in pyridine (225 mL) was added paraformaldehyde (15.7 g, 514.3 mmol) and a 40% Triton-B solution (in methanol) (14.4 mL). Then the reaction mixture stirred at room temperature for 16 h. At this time, the reaction mixture was diluted with water (10 mL) and extracted with ethyl acetate (300 mL). The organic layer was washed with a 2N aqueous hydrochloric acid solution (2×200 mL), water (2×100 mL), sodium bicarbonate (2×50 mL), a saturated aqueous sodium chloride solution (50 mL), dried over anhydrous sodium sulfate, and concentrated in vacuo. Flash chromatography afforded 2-(4-bromo-phenyl)-3-hydroxy-2-methyl-propionitrile as colorless oil (25.9 g, 84%).

후처리

  1. extractionextracted with ethyl acetate (300 mL)
  2. washThe organic layer was washed with a 2N aqueous hydrochloric acid solution (2×200 mL), water (2×100 mL), sodium bicarbonate (2×50 mL)
  3. dry with materiala saturated aqueous sodium chloride solution (50 mL), dried over anhydrous sodium sulfate
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9230fff9fd19497abd20a90346a45015
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722661B2

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