Hexane → 3,6-Bis(diphenylphosphinyl)pyridazine

HRID 1065631

반응식

HRID 1065631 반응식
Cl[C:2]1[N:3]=[N:4][C:5](Cl)=[CH:6][CH:7]=1.[C:9]1([P:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[O:16]C)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[CH3:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29]>ClC1C=CC=CC=1Cl>[C:9]1([P:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)([C:2]2[N:3]=[N:4][C:5]([P:15]([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=3)([C:26]3[CH:25]=[CH:24][CH:29]=[CH:28][CH:27]=3)=[O:16])=[CH:6][CH:7]=2)=[O:16])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1

참가 물질

5

반응물 3

HCID 8058HexaneHCID 673313,6-DichloropyridazineHCID 77636Methoxydiphenylphosphine

생성물 1

HCID 205394883,6-Bis(diphenylphosphinyl)pyridazine

시약·촉매·용매 1

HCID 72391,2-Dichlorobenzene용매

실험 절차

To a stirred, refluxing solution of 3.00 g of 3,6-dichloropyridazine in 50 ml of o-dichlorobenzene under nitrogen was added dropwise 10.00 g of methyl diphenylphosphinite. After the addition was completed, the mixture was refluxed for 7 hours and then cooled. The cooled mixture was mixed with excess hexane; the oil which formed slowly crystallized. The resultant solid was separated by filtration, washed with hexane, and recrystallized twice from ethanol with decolorizing charcoal treatment to give 0.93 g of 3,6-bis(diphenylphosphinyl)pyridazine (shown by formula in claim 7) as slightly off-white crystals, mp 248°-251.5° C. Anal. Calcd for C28H22N2O2P2 : C, 70.00; H, 4.62; N, 5.83; P, 12.89. Found: C, 69.72; H, 4.92; N, 5.78; P, 12.82.

후처리

  1. additionAfter the addition
  2. temperaturethe mixture was refluxed for 7 hours
  3. temperaturecooled
  4. customthe oil which formed slowly
  5. customcrystallized
  6. customThe resultant solid was separated by filtration
  7. washwashed with hexane
  8. customrecrystallized twice from ethanol with decolorizing charcoal treatment

출처 및 근거

ORD 기록
ord-511b63dc2056448fbe0e45e1d96a37b5
출처 데이터셋
uspto-grants-1982_05
특허 번호
US04330461

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