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Triphenylphosphine → HCID 69314044、化合物

HRID 2222268
ノート
印刷プレビュー

反応式

HRID 2222268 の反応式
I[C:2]1[CH:6]=[CH:5][N:4]([Si:7]([CH:14]([CH3:16])[CH3:15])([CH:11]([CH3:13])[CH3:12])[CH:8]([CH3:10])[CH3:9])[CH:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.Br[C:37]1([Zn])[CH:42]=[CH:41][CH:40]=[CH:39][NH:38]1>C1COCC1.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH:8]([Si:7]([CH:14]([CH3:16])[CH3:15])([CH:11]([CH3:13])[CH3:12])[N:4]1[CH:5]=[CH:6][C:2]([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][N:38]=2)=[CH:3]1)([CH3:10])[CH3:9]
参加物反応条件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 11776TriphenylphosphineHCID 142471191H-Pyrrole, 3-iodo-1-[tris(1-methylethyl)silyl]-HCID 178528051HCID 178528051、化合物

生成物 1

HCID 69314044HCID 69314044、化合物

試薬・触媒・溶媒 2

HCID 178418397HCID 178418397、化合物触媒HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
70 °C

実験手順

A solution of 3-iodo-1-(triisopropylsilyl)-1H-pyrrole (11.0 g, 2.87 mmol), triphenylphosphine (27 mg, 0.103 mmol), and tetrakis(triphenylphosphine)palladium(0) (80 mg, 0.069 mmol) in THF (20 mL) was degassed with Ar (g) for 15 min, then 2-bromo(pyridin-2-yl)zinc (1.5 mL of 0.5M solution, 5.74 mmol) was added and degassing continued a further 15 min. The reaction was stirred at 70° C. for 5 h and monitored by LC/MS. The reaction mixture was quenched with H2O (40 mL) then extracted with EtOAc (3×25 mL) and the combined organic extracts washed with brine. The organic phase was dried over Na2SO4, concentrated in vacuo and the crude residue was chromatographed on silica gel eluting with EtOAc:hexane (1:9) to afford 2-[1-(triisopropylsilyl)-1H-pyrrol-3-yl]pyridine as a clear oil which was used below without further purification.

後処理

  1. customdegassing
  2. customThe reaction mixture was quenched with H2O (40 mL)
  3. extractionthen extracted with EtOAc (3×25 mL)
  4. washthe combined organic extracts washed with brine
  5. dry with materialThe organic phase was dried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. customthe crude residue was chromatographed on silica gel eluting with EtOAc:hexane (1:9)

出典と根拠

ORDレコード
ord-78dde0ad53bc47f4989329e7237990f0
出典データセット
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07371767B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート