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Methanol → Methyl 2-(3,5-difluorophenyl)-2-hydroxyacetate

HRID 1037754
ノート
印刷プレビュー

反応式

HRID 1037754 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:9]([OH:13])[C:10]([OH:12])=[O:11])[CH:5]=[C:6]([F:8])[CH:7]=1.B(O)(O)O.[CH3:18]O>>[F:1][C:2]1[CH:3]=[C:4]([CH:9]([OH:13])[C:10]([O:12][CH3:18])=[O:11])[CH:5]=[C:6]([F:8])[CH:7]=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 3

HCID 887MethanolHCID 7628Boric AcidHCID 5886483,5-Difluoromandelic acid

生成物 1

HCID 22312159Methyl 2-(3,5-difluorophenyl)-2-hydroxyacetate

実験手順

25.0 g of 3,5-difluorophenylhydroxyacetic acid (D2) are dissolved in 325 ml of methanol. 3.9 g of boric acid are subsequently added, and the reaction mixture is stirred at room temperature for 18 hours. The resultant solution is then evaporated to dryness. The residue is extracted using 100 ml of ethyl acetate and 100 ml of water. The aqueous phase is subsequently extracted twice with 50 ml of ethyl acetate each time. The combined organic phases are dried over sodium sulfate and filtered. The filtrate is evaporated to dryness in vacuo, giving 25.5 g of the title compound as crude product. Recrystallisation from 17 ml of ethyl acetate and 170 ml of cyclohexane give 23.5 g of the pure compound C2 having a melting point of 61.8° C. (MS 201.9 (M+)).

後処理

  1. customThe resultant solution is then evaporated to dryness
  2. extractionThe residue is extracted
  3. extractionThe aqueous phase is subsequently extracted twice with 50 ml of ethyl acetate each time
  4. dry with materialThe combined organic phases are dried over sodium sulfate
  5. filtrationfiltered
  6. customThe filtrate is evaporated to dryness in vacuo

出典と根拠

ORDレコード
ord-5f9aac7c55a047b18bbdcba136ebae20
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08546613B2

反応ノート

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