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Pentanal → 1-(3,5-Difluorophenyl)pentan-1-ol

HRID 1741551
ノート
印刷プレビュー

反応式

HRID 1741551 の反応式
[CH:1](=[O:6])[CH2:2][CH2:3][CH2:4][CH3:5].Br[C:8]1[CH:13]=[C:12]([F:14])[CH:11]=[C:10]([F:15])[CH:9]=1.[Mg].[Cl-].[NH4+]>CCOCC.C1COCC1>[F:15][C:10]1[CH:9]=[C:8]([CH:1]([OH:6])[CH2:2][CH2:3][CH2:4][CH3:5])[CH:13]=[C:12]([F:14])[CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 8063PentanalHCID 25517Ammonium ChlorideHCID 1363131-Bromo-3,5-difluorobenzeneHCID 5462224Magnesium

生成物 1

HCID 225984431-(3,5-Difluorophenyl)pentan-1-ol収率 116%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

A solution of pentanal (19.0 g, 0.22 mol) in dry ether (75 ml) was added dropwise to a stirred solution of the Grignard reagent at room temperature, under dry nitrogen, prepared from 1-bromo-3,5-difluorobenzene (50.2 g, 0.26 mol) and magnesium (7.25 g, 0.30 mol) in dry THF (100 ml). The stirred mixture was heated under reflux for 2 h, cooled and a saturated solution of ammonium chloride (300 ml) was added. The product was extracted into ether (twice), and the combined ethereal extracts were washed with water and dried (MgSO4). The solvent was removed in vacuo to give a pale-orange liquid (51.1 g) which was distilled to yield a colourless liquid. Smaller quantities of crude product were purified by column chromatography (silica gel/dichloromethane) to yield a colourless liquid (92%).

後処理

  1. temperatureThe stirred mixture was heated
  2. temperatureunder reflux for 2 h
  3. temperaturecooled
  4. extractionThe product was extracted into ether (twice), and the combined ethereal extracts
  5. washwere washed with water
  6. dry with materialdried (MgSO4)
  7. customThe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-b7dee7ff80284a43b6cf00918591f552
出典データセット
uspto-grants-1994_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05334327

反応ノート

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