Pyrrolidine → 6-cyano-3,4-dihydro-2,2-bis(methoxymethyl)-2H-1-benzopyran-4-one

HRID 862478노트

반응식

HRID 862478 반응식
[CH3:1][C:2]([C:4]1[CH:9]=[C:8]([C:10]#[N:11])[CH:7]=[CH:6][C:5]=1[OH:12])=[O:3].N1CCCC1.[CH3:18][O:19][CH2:20][C:21](=O)[CH2:22][O:23][CH3:24]>C1(C)C=CC=CC=1>[C:10]([C:8]1[CH:7]=[CH:6][C:5]2[O:12][C:21]([CH2:22][O:23][CH3:24])([CH2:20][O:19][CH3:18])[CH2:1][C:2](=[O:3])[C:4]=2[CH:9]=1)#[N:11]

참가 물질

5

반응물 3

HCID 31268PyrrolidineHCID 15018881,3-DimethoxyacetoneHCID 123328323-Acetyl-4-hydroxybenzonitrile

생성물 1

HCID 107301156-cyano-3,4-dihydro-2,2-bis(methoxymethyl)-2H-1-benzopyran-4-one

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

5-Cyano-2-hydroxyacetophenone (13.57 g) was dissolved in toluene (120 ml), and pyrrolidine (6 ml) and 1,3-dimethoxy-2-propanone (15 ml) were added. The mixture was refluxed under heating for 1 hour while removing the generated water. After cooling, the reaction mixture was diluted with ethyl acetate, washed with dilute hydrochloric acid, an aqueous solution of sodium hydrogencarbonate and brine in order, and dried over anhydrous magnesium sulfate. The solvent was distilled away and the residue obtained was purified by silica gel column chromatography (ethyl acetate:hexane=2:8) to give 13.0 g of 6-cyano-3,4-dihydro-2,2-bis(methoxymethyl)-2H-1-benzopyran-4-one.

후처리

  1. temperatureThe mixture was refluxed
  2. temperatureunder heating for 1 hour
  3. customwhile removing the generated water
  4. temperatureAfter cooling
  5. additionthe reaction mixture was diluted with ethyl acetate
  6. washwashed with dilute hydrochloric acid
  7. dry with materialan aqueous solution of sodium hydrogencarbonate and brine in order, and dried over anhydrous magnesium sulfate
  8. distillationThe solvent was distilled away
  9. customthe residue obtained
  10. customwas purified by silica gel column chromatography (ethyl acetate:hexane=2:8)

출처 및 근거

ORD 기록
ord-f72d45b42c804179b1422b549a0c6cc5
출처 데이터셋
uspto-grants-1998_02
특허 번호
US05719155

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