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Hexane → (R)-4-Bromo-isopropylidenebutane-1,2-diol

HRID 1087393
ノート
印刷プレビュー

反応式

HRID 1087393 の反応式
[C:1](=[C:4]([OH:10])[C@H:5]([OH:9])[CH2:6][CH2:7]O)([CH3:3])[CH3:2].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:30]N1C(=O)CCC1=O.CCCCCC>C(Cl)Cl>[Br:30][CH2:7][CH2:6][C@@H:5]([OH:9])[C:4](=[C:1]([CH3:3])[CH3:2])[OH:10]
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 4

HCID 8058HexaneHCID 11776TriphenylphosphineHCID 67184N-bromobutanimideHCID 86744937(R)-isopropylidenebutane-1,2,4-triol

生成物 1

HCID 18595859(R)-4-Bromo-isopropylidenebutane-1,2-diol収率 47%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

(R)-Isopropylidenebutane-1,2,4-triol (0.3 g, 2.05 mmol) and triphenylphosphine (0.63 g, 2.4 mmol) were dissolved in methylene chloride (5 ml) and cooled to 0° C. and N-bromosuccinimide (0.38 g, 2.16 mmol) was added in small portions with stirring. After additional 1 h of stirring at 0° C. hexane (15 ml) was added and the resulting precipitate was removed by filtration and washed twice with hexane (2×5 ml). The combined hexane solution was passed through a short column of silica gel (5 g). Elution with hexane (15 ml) gave after evaporation and distillation the title compound as a colourless oil (0.2 g, 0.96 mmol, 47%): b.p. 74°-76° C. at 2.7 kPa (20 mm Hg), nD20 =1.4630. {α}D20 =+27.7° (c=20, CHCl3).

後処理

  1. additionwas added
  2. customthe resulting precipitate was removed by filtration
  3. washwashed twice with hexane (2×5 ml)
  4. washElution with hexane (15 ml)
  5. customgave

出典と根拠

ORDレコード
ord-54db96131c5b4e38917f5fd2aaac0b74
出典データセット
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05036071

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