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Tetraethyl [[1,1'-biphenyl]-4,4'-diylbis(methylene)]bis(phosphonate) → HCID 67429829、化合物

HRID 1660682
ノート
印刷プレビュー

反応式

HRID 1660682 の反応式
[CH3:1][C:2]([CH3:5])([O-])[CH3:3].[K+].[C:7]1([N:13]2[C:26]3[CH:25]=[CH:24][C:23]([CH:27]=O)=[CH:22][C:21]=3[S:20](=[O:30])(=[O:29])[C:19]3[C:14]2=[CH:15][CH:16]=[CH:17][CH:18]=3)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.C(OP([CH2:39][C:40]1[CH:45]=[CH:44][C:43]([C:46]2[CH:51]=[CH:50][C:49]([CH2:52]P(OCC)(OCC)=O)=[CH:48][CH:47]=2)=[CH:42][CH:41]=1)(=O)OCC)C>CS(C)=O.C(Cl)Cl>[C:7]1([N:13]2[C:26]3[CH:25]=[CH:3][C:2]([CH:5]=[CH:52][C:49]4[CH:48]=[CH:47][C:46]([C:43]5[CH:42]=[CH:41][C:40]([CH:39]=[CH:27][C:23]6[CH:24]=[CH:25][C:26]7[N:13]([C:7]8[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=8)[C:14]8[C:19]([S:20](=[O:30])(=[O:29])[C:21]=7[CH:22]=6)=[CH:18][CH:17]=[CH:16][CH:15]=8)=[CH:45][CH:44]=5)=[CH:51][CH:50]=4)=[CH:1][C:21]=3[S:20](=[O:30])(=[O:29])[C:19]3[C:14]2=[CH:15][CH:16]=[CH:17][CH:18]=3)[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 635132Tetraethyl [[1,1'-biphenyl]-4,4'-diylbis(methylene)]bis(phosphonate)HCID 23665647Potassium tert-butoxideHCID 59609624HCID 59609624、化合物

生成物 1

HCID 67429829HCID 67429829、化合物

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒
HCID 6344
Dichloromethane
溶媒

実験手順

2.28 g (19.9 mmol) of potassium tert-butoxide and then 5.90 g (17.6 mmol) of 10-phenyl-5,5-dioxophenothiazine-3-carbaldehyde (Example 21) were added under nitrogen at room temperature with stirring to a solution of 4.00 g (8.80 mmol) of diethyl[4′-(diethoxyphosphorylmethyl)biphenyl-4-ylmethyl]phosphonate in 45 ml of dimethyl sulfoxide dried over molecular sieve. After stirring at room temperature for 72 h, the reaction solution was diluted with 200 ml of methanol and stirred for a further 1 h. The precipitate was filtered off, washed with 500 ml of methanol and dried at 80° C. under reduced pressure. The crude product (5.44 g) was recrystallized in 250 ml of o-dichlorobenzene. The crystals were filtered off with suction, washed successively with o-dichlorobenzene and ethanol, filtered off with suction and dried at 80° C. under reduced pressure. After solvent residues had been removed in high vacuum (2×10−5 mbar) at 250° C., 4.35 g (60% of theory) of yellow microcrystals having a melting point of 392° C. were obtained, whose solution in methylene chloride fluoresced at λ=456 nm.

後処理

  1. customdried over molecular sieve
  2. additionthe reaction solution was diluted with 200 ml of methanol
  3. stirringstirred for a further 1 h
  4. filtrationThe precipitate was filtered off
  5. washwashed with 500 ml of methanol
  6. customdried at 80° C. under reduced pressure
  7. customThe crude product (5.44 g) was recrystallized in 250 ml of o-dichlorobenzene
  8. filtrationThe crystals were filtered off with suction
  9. washwashed successively with o-dichlorobenzene and ethanol
  10. filtrationfiltered off with suction
  11. customdried at 80° C. under reduced pressure
  12. customAfter solvent residues had been removed in high vacuum (2×10−5 mbar) at 250° C.
  13. customwere obtained

出典と根拠

ORDレコード
ord-b2856ae2c79a46d18317ca78fc89ea34
出典データセット
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08029919B2

反応ノート

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