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Triphenylphosphine → HCID 86749136, 화합물

HRID 2259507
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HRID 2259507 반응식
[Cl:1][C:2]1[O:10][C:9]2[C:4](=[N:5][C:6]([CH3:11])=[CH:7][CH:8]=2)[C:3]=1[Cl:12].[Br:13]N1C(=O)CCC1=O.[C:21]1([P:27]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C(Cl)(Cl)(Cl)Cl.CC#N.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>[Br-:13].[Cl:1][C:2]1[O:10][C:9]2[C:4](=[N:5][C:6]([CH2:11][P+:27]([C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)([C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)[C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)=[CH:7][CH:8]=2)[C:3]=1[Cl:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 11776TriphenylphosphineHCID 67184N-bromobutanimideHCID 19002930HCID 19002930, 화합물

생성물 1

HCID 86749136HCID 86749136, 화합물수율 77%

시약·촉매·용매 3

HCID 7187Benzoyl Peroxide촉매HCID 5943Carbon Tetrachloride
용매
HCID 6342Acetonitrile용매

실험 절차

To a solution of 2,3-dichloro-5-methylfurano[3,2-b]pyridine (0.5 g, 2.47 mmol) in CCl4 (15 mL) was added N-bromosuccinimide (0.44 g, 2.47 mmol) and benzoyl peroxide (2 mg). The mixture was stirred and photolyzed using a sun lamp for 1 hr. The resulting mixture was cooled and filtered through celite. Evaporation of the filtrate gave an oil which was then dissolved in CH3CN (10 mL). Triphenylphosphine (1.29 g, 4.94 mmol) was added and the mixture was stirred at r.t. for 20 hr. The solvent was removed and the residue was triturated with ether to afford 1 g (77%) of the title compound after filtration.

후처리

  1. customfor 1 hr
  2. temperatureThe resulting mixture was cooled
  3. filtrationfiltered through celite
  4. customEvaporation of the filtrate
  5. customgave an oil which
  6. stirringthe mixture was stirred at r.t. for 20 hr
  7. customThe solvent was removed
  8. customthe residue was triturated with ether

출처 및 근거

ORD 기록
ord-a8679e05131d41c39a628cf2d431498d
출처 데이터셋
uspto-grants-1995_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05472964

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