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Ammonia → 1-Methoxy-4-(4-hydroxybutyl)cyclohexa-1,4-diene

HRID 1494094
ノート
印刷プレビュー

反応式

HRID 1494094 の反応式
N.[OH:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1.[Na]>C(O)C>[CH3:14][O:13][C:10]1[CH2:11][CH:12]=[C:7]([CH2:6][CH2:5][CH2:4][CH2:3][OH:2])[CH2:8][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 222AmmoniaHCID 976604-(4-Methoxyphenyl)butan-1-olHCID 5360545Sodium

生成物 1

HCID 103523271-Methoxy-4-(4-hydroxybutyl)cyclohexa-1,4-diene

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Ammonia (75 mL) is liquified in a flask at -40° and a solution of 5 g (28 mmol) of p-(4-hydroxybutyl)anisole in 25 mL ethanol is added. 2.76 g (0.12 mmol) of sodium is added in small pieces over 1 hour. The blue solution is then stirred at -40° for 10 minutes during which time the solution decolorizes with the formation of a white precipitate. The reaction is quenched using 5.88 g solid ammonium chloride followed by 25 mL water. The solvent is evaporated under a stream of nitrogen and then poured into brine and extracted with ether (4×100 mL). The organic extracts are combined, dried, filtered and subjected to evaporation to give 1-methoxy-4-(4-hydroxybutyl)cyclohexa1,4-diene as an oil.

後処理

  1. customThe reaction is quenched
  2. customThe solvent is evaporated under a stream of nitrogen
  3. additionpoured into brine
  4. extractionextracted with ether (4×100 mL)
  5. customdried
  6. filtrationfiltered
  7. customsubjected to evaporation

出典と根拠

ORDレコード
ord-68b821aaab3e4e65ba13300546bc3354
出典データセット
uspto-grants-1991_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05025025

反応ノート

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