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

HRID 446360
ノート
印刷プレビュー

反応式

HRID 446360 の反応式
CSC.B.[Br:5][CH2:6][C:7]1[CH:8]=[C:9]([CH2:14][C:15](O)=[O:16])[CH:10]=[C:11]([F: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]([F:13])[CH:12]=1
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

4

反応物 2

HCID 12423031(Dimethyl sulfide)trihydroboronHCID 579890372-(3-(Bromomethyl)-5-fluorophenyl)acetic acid

生成物 1

HCID 579893452-(3-(Bromomethyl)-5-fluorophenyl)ethanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

Borane dimethyl sulfide complex (2M in THF, 26.3 mL) was added dropwise over 10 minutes to a solution of 2-(3-(bromomethyl)-5-fluorophenyl)acetic acid [Aromatic Intermediate 4, step a] (6.5 g) in THF (120 mL) at 0° C. The mixture was stirred at 0° C. for 10 minutes and then at 20° C. for 1 hour. The reaction mixture was quenched by dropwise addition of methanol and the solvents were removed under reduced pressure. The crude product was purified by flash silica chromatography using 30% ethyl acetate in isohexane. Fractions containing the product were concentrated to dryness to afford the titled compound. Yield 4.70 g.

後処理

  1. waitat 20° C. for 1 hour
  2. customThe reaction mixture was quenched by dropwise addition of methanol
  3. customthe solvents were removed under reduced pressure
  4. customThe crude product was purified by flash silica chromatography
  5. additionFractions containing the product
  6. concentrationwere concentrated to dryness

出典と根拠

ORDレコード
ord-fcabc19157d144a8a8f0082cab8725a8
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08476265B2

反応ノート

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