Triphenylphosphine → 2-(5-Bromopent-1-ynyl)pyridine

HRID 334634ノート

反応式

HRID 334634 の反応式
[Br:1]Br.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[N:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[C:28]#[C:29][CH2:30][CH2:31][CH2:32]O>C(Cl)Cl>[Br:1][CH2:32][CH2:31][CH2:30][C:29]#[C:28][C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][N:22]=1

参加物

5

反応条件

温度
5 °C

実験手順

Br2 (1.11 mL, 21.4 mmol) was added to a solution of triphenylphosphine (8.30 g, 30.7 mmol) in DCM (40 mL) at −5° C. A solution of 5-pyridin-2-yl-pent-4-yn-1-ol (3.00, 18.6 mmol) in DCM (10 mL) was added dropwise to the reaction mixture in order to maintain a temperature lower than 5° C. The reaction mixture was stirred for 5 hours at −10° C. and was quenched with a saturated solution of NaHCO3. The aqueous phase was extracted with DCM. The resulting organic phase was washed with brine, dried over MgSO4, filtered and evaporated. The crude residue was purified by flash chromatography (DCM/MeOH 99.5:0.5) to yield 2-(5-bromo-pent-1-ynyl)-pyridine (1.20 g, 5.35 mmol, 29%) with a purity of 50%.

後処理

  1. customwas quenched with a saturated solution of NaHCO3
  2. extractionThe aqueous phase was extracted with DCM
  3. washThe resulting organic phase was washed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude residue was purified by flash chromatography (DCM/MeOH 99.5:0.5)

出典と根拠

ORDレコード
ord-9313c62210014996a25cb65f7ca1bee0
出典データセット
uspto-grants-2014_11
特許番号
US08883826B2

反応ノート

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