Acetic Acid → 5-Bromo-2-pyridinepropanol

HRID 2108035

反応式

HRID 2108035 の反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]#[C:9][CH2:10][OH:11])=[N:6][CH:7]=1.C(O)(=O)C>N1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][CH2:10][OH:11])=[N:6][CH:7]=1

参加物

4

実験手順

To a suspension of 3-(5-bromo-2-pyridinyl)-2-propyn-1-ol (0.5 g) and dipotassium azadicarboxylate (3.66 g) in pyridine (40 ml) was added acetic acid (2 ml) and the mixture stirred at room temperature for 24 h, with further additions of acetic acid after 2 h (0.16 ml) and 17 h (2.16 ml). As reduction had only partially gone to completion, further dipotassium azadicarboxylate (3.2 g) and acetic acid (1.86 ml) were added, and stirring continued for 17 h. The mixture was quenched with water (15 ml) and evaporated in vacuo. The residue was co-evaporated with toluene (15 ml) and the residue partitioned between 8% sodium bicarbonate solution (60 ml) and ethyl acetate (60 ml) and the organic phase dried and evaporated in vacuo. The oily residue was purified by FCC using ether and ether-methanol (5%) eluants to afford the title compound as a yellow oil (0.42 g).

後処理

  1. additionwere added
  2. customThe mixture was quenched with water (15 ml)
  3. customevaporated in vacuo
  4. customthe residue partitioned between 8% sodium bicarbonate solution (60 ml) and ethyl acetate (60 ml)
  5. customthe organic phase dried
  6. customevaporated in vacuo
  7. customThe oily residue was purified by FCC

出典と根拠

ORDレコード
ord-65d6daa4aa4342ff8a2038e551438cdb
出典データセット
uspto-grants-1990_06
特許番号
US04937251

関連ノート

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