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(Dimethyl sulfide)trihydroboron → 2-(2-Chloro-3-(hydroxymethyl)phenyl)ethanol

HRID 471184
ノート
印刷プレビュー

反応式

HRID 471184 の反応式
B.CSC.[C:5]([CH2:8][C:9]1[C:10]([Cl:18])=[C:11]([CH:15]=[CH:16][CH:17]=1)[C:12](O)=[O:13])(O)=[O:6]>C1COCC1>[Cl:18][C:10]1[C:11]([CH2:12][OH:13])=[CH:15][CH:16]=[CH:17][C:9]=1[CH2:8][CH2:5][OH:6]
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 579889673-(Carboxymethyl)-2-chlorobenzoic acid

生成物 1

HCID 579892482-(2-Chloro-3-(hydroxymethyl)phenyl)ethanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of borane-methyl sulfide complex (2M in THF, 20 mL) was added portionwise over 5 minutes to a suspension of 3-(carboxymethyl)-2-chlorobenzoic acid (example 80, step b) (4.11 g) in dry THF (100 mL) at room temperature. The resulting effervescing suspension was stirred at room temperature for 30 minutes, then heated to reflux for 60 minutes, and allowed to cool to room temperature overnight. The mixture was quenched by the portionwise addition of methanol (15 mL) over 15 minutes. The mixture was diluted further with methanol to give a solution, which was then concentrated in vacuo to give a syrup. The syrup was purified by flash chromatography on silica eluted with 2% methanol in dichloromethane to the afford the crude subtitled compound as a white solid. Yield 1.44 g.

後処理

  1. temperatureheated
  2. temperatureto reflux for 60 minutes
  3. temperatureto cool to room temperature overnight
  4. customThe mixture was quenched by the portionwise addition of methanol (15 mL) over 15 minutes
  5. additionThe mixture was diluted further with methanol
  6. customto give a solution, which
  7. concentrationwas then concentrated in vacuo
  8. customto give a syrup
  9. customThe syrup was purified by flash chromatography on silica
  10. washeluted with 2% methanol in dichloromethane to the

出典と根拠

ORDレコード
ord-18378592b1a34f529405b56eb595f303
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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