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(Dimethyl sulfide)trihydroboron → 2-(3-(Bromomethyl)-5-chlorophenyl)ethanol

HRID 471100
ノート
印刷プレビュー

反応式

HRID 471100 の反応式
B.CSC.[Br:5][CH2:6][C:7]1[CH:8]=[C:9]([CH2:14][C:15](O)=[O:16])[CH:10]=[C:11]([Cl:13])[CH:12]=1>C1COCC1>[Br:5][CH2:6][C:7]1[CH:8]=[C:9]([CH2:14][CH2:15][OH:16])[CH:10]=[C:11]([Cl:13])[CH:12]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 12423031(Dimethyl sulfide)trihydroboronHCID 579893592-(3-(Bromomethyl)-5-chlorophenyl)acetic acid

生成物 1

HCID 579892922-(3-(Bromomethyl)-5-chlorophenyl)ethanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of borane-methyl sulfide complex (2 M in THF, 2.8 mL) was added portionwise over 5 minutes to a solution of 2-(3-(bromomethyl)-5-chlorophenyl)acetic acid (example 52, step a) (0.73 g) in dry THF (10 mL) at room temperature. The resulting effervescing solution was stirred for 1 hour, then cooled in ice-water and quenched by the portionwise addition of methanol (3 mL) over 5 minutes. The solution was stirred at room temperature for a further 20 minutes and then concentrated in vacuo. The residue was purified by flash chromatography on silica eluted with 25% ethyl acetate in isohexane to afford the crude subtitled compound as a white solid. Yield 0.46 g.

後処理

  1. customquenched by the portionwise addition of methanol (3 mL) over 5 minutes
  2. stirringThe solution was stirred at room temperature for a further 20 minutes
  3. concentrationconcentrated in vacuo
  4. customThe residue was purified by flash chromatography on silica
  5. washeluted with 25% ethyl acetate in isohexane

出典と根拠

ORDレコード
ord-9a379f81a1e54a6da24236c547216224
出典データセット
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08629271B2

反応ノート

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