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Sodium → (S)-1-(4-chloro-3-fluorophenyl)propane-1,3-diol

HRID 2365805
ノート
印刷プレビュー

反応式

HRID 2365805 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]2[O:10][C@@H:9]2[CH2:11][OH:12])=[CH:4][C:3]=1[F:13].[Na]>COCCOC.CCOCC>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]([OH:10])[CH2:9][CH2:11][OH:12])=[CH:4][C:3]=1[F:13]
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

5

反応物 2

HCID 5360545SodiumHCID 86696658((2R,3R)-3-(4-chloro-3-fluorophenyl)oxiran-2-yl)methanol

生成物 1

HCID 86696659(S)-1-(4-chloro-3-fluorophenyl)propane-1,3-diol収率 98.55%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 80711,2-Dimethoxyethane溶媒

反応条件

温度
0 °C

実験手順

((2R,3R)-3-(4-Chloro-3-fluorophenyl)oxiran-2-yl)methanol (10.55 g, 52.07 mmol) was dissolved in 1,2-dimethoxyethane (150 mL) and cooled to 0° C. Sodium bis(2-methohyethoxy) aluminum hydride (“Red-Al”) (17.46 mL, 57.28 mmol) was added dropwise. The mixture was agitated for 3 hours at room temperature, diluted with ether (250 mL) and quenched with HCl solution (20 mL, 6M HCl+60 mL water). After agitating for 30 minutes, the aqueous phase was separated and extracted twice with ethyl acetate. The combined organics were washed with brine, dried with MgSO4, and evaporated to give (S)-1-(4-chloro-3-fluorophenyl)propane-1,3-diol (10.5 g, 51.31 mmol, 98.55% yield) as thick oil.

後処理

  1. customquenched with HCl solution (20 mL, 6M HCl+60 mL water)
  2. stirringAfter agitating for 30 minutes
  3. customthe aqueous phase was separated
  4. extractionextracted twice with ethyl acetate
  5. washThe combined organics were washed with brine
  6. dry with materialdried with MgSO4
  7. customevaporated

出典と根拠

ORDレコード
ord-41717bdf14184c7c9c8816f815420a04
出典データセット
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08697715B2

反応ノート

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