Chloride → 2-Triethylsilyl-5-phenyl-4-furaldehyde

HRID 1681526

反応式

HRID 1681526 の反応式
[CH2:1]([Si:3]([CH2:13][CH3:14])([CH2:11][CH3:12])[C:4]1[O:5][CH:6]=[C:7]([CH:9]=[O:10])[CH:8]=1)[CH3:2].[Li]N(C)CCN(C)C.FC(F)(F)S(O[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)(=O)=O.[Cl-]>[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH2:13]([Si:3]([CH2:11][CH3:12])([CH2:1][CH3:2])[C:4]1[O:5][C:6]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)=[C:7]([CH:9]=[O:10])[CH:8]=1)[CH3:14]

参加物

6

反応物 4

HCID 312ChlorideHCID 548641Phenyl TrifluoromethanesulfonateHCID 108784383-Furancarboxaldehyde, 5-(triethylsilyl)-HCID 178506926HCID 178506926、化合物

生成物 1

HCID 194331442-Triethylsilyl-5-phenyl-4-furaldehyde

試薬・触媒・溶媒 1

HCID 11979704Tetrakis(triphenylphosphine)palladium触媒

実験手順

Treatment of 2-triethylsilyl-4-furaldehyde with lithio N,N,N'-trimethylethylenediamine, followed by phenyl trifluoromethanesulfonate in the presence of anhydrous zinz chloride and tetrakis (triphenylphosphine) palladium (o) and work up gives the titled aldehyde.

出典と根拠

ORDレコード
ord-7ba055d73a604357b1a6c27c8821569c
出典データセット
uspto-grants-1992_12
特許番号
US05171863

関連ノート

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