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Acetyl chloride → Methyl 2-(3-acetyl-4-hydroxyphenyl)propionate

HRID 26680
ノート
印刷プレビュー

反応式

HRID 26680 の反応式
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH3:14])[C:10]([O:12][CH3:13])=[O:11])=[CH:5][CH:4]=1.[C:15](Cl)(=[O:17])[CH3:16].B(Cl)(Cl)Cl>ClCCl.[Ti](Cl)(Cl)(Cl)Cl>[C:15]([C:4]1[CH:5]=[C:6]([CH:9]([CH3:14])[C:10]([O:12][CH3:13])=[O:11])[CH:7]=[CH:8][C:3]=1[OH:2])(=[O:17])[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6367Acetyl chlorideHCID 25135Boron TrichlorideHCID 12398855Methyl 2-(4-methoxyphenyl)propanoate

生成物 1

HCID 21322000Methyl 2-(3-acetyl-4-hydroxyphenyl)propionate

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒HCID 6344Dichloromethane溶媒

実験手順

Titanium tetrachloride (82.3 mls) was added dropwise to a stirred solution of methyl 2-(4-methoxyphenyl)propionate (25 g) in dry dichloromethane (250 mls), cooled in an ice/salt-bath, at a rate sufficient to maintain the temperature between -10° C. and -5° C. The mixture was stirred for 10 minutes and acetyl chloride (10 g) was added dropwise at a rate sufficient to maintain the temperature below 0° C. The solution was stirred at -5° C. for 11/2 hours when boron trichloride (15 mls) was added. Stirring was continued for 1/2 hour at +3° C. before pouring on to crushed ice/concentrated hydrochloric acid and separating the two phases. The aqueous phase was extracted with ether (3x) and the combined organic extracts were washed with saturated sodium bicarbonate solution, saturated brine solution, and dried over anhydrous magnesium sulphate. Evaporation of the solvent yielded the crude product as a pale yellow oil. Vacuum distillation furnished a pale yellow oil bp 120°-125° C./0.15 mm (16.2 g; 59%)

後処理

  1. temperaturecooled in an ice/salt-bath, at a rate sufficient
  2. temperatureto maintain the temperature between -10° C. and -5° C
  3. temperatureto maintain the temperature below 0° C
  4. additionwas added
  5. stirringStirring
  6. waitwas continued for 1/2 hour at +3° C.
  7. additionbefore pouring on
  8. customto crushed ice/concentrated hydrochloric acid
  9. customseparating the two phases
  10. extractionThe aqueous phase was extracted with ether (3x)
  11. washthe combined organic extracts were washed with saturated sodium bicarbonate solution, saturated brine solution
  12. dry with materialdried over anhydrous magnesium sulphate
  13. customEvaporation of the solvent
  14. customyielded the crude product as a pale yellow oil
  15. distillationVacuum distillation

出典と根拠

ORDレコード
ord-bf78a7c0cbc341b7b26a0654b5d987b7
出典データセット
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04151179

反応ノート

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