Chloroacetyl chloride → 4-Benzyl-6-(4-bromo-phenyl)-morpholin-3-one

HRID 2063359ノート

反応式

HRID 2063359 の反応式
Cl[CH2:2][C:3](Cl)=[O:4].[CH2:6]([NH:13][CH2:14][CH:15]([C:17]1[CH:22]=[CH:21][C:20]([Br:23])=[CH:19][CH:18]=1)[OH:16])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.C(N(CC)CC)C.C[O-].[Na+]>C1(C)C=CC=CC=1.CO>[CH2:6]([N:13]1[CH2:14][CH:15]([C:17]2[CH:18]=[CH:19][C:20]([Br:23])=[CH:21][CH:22]=2)[O:16][CH2:2][C:3]1=[O:4])[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

参加物

7

反応物 4

HCID 6577Chloroacetyl chlorideHCID 8471TriethylamineHCID 10942334Sodium MethoxideHCID 580978892-Benzylamino-1-(4-bromo-phenyl)-ethanol2 回

生成物 1

HCID 580978854-Benzyl-6-(4-bromo-phenyl)-morpholin-3-one収率 86%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 1140Toluene溶媒3 回

実験手順

After addition of chloroacetyl chloride (8.49 g, 75.2 mmol) in toluene (30 ml) to a ice-cooled solution of 2-benzylamino-1-(4-bromo-phenyl)-ethanol (intermediate 31, 21.85 g, 71.4 mmol) in toluene (300 ml), a solution of triethylamine (10.25 g, 101 mmol) in toluene (20 ml) was added to the mixture and stirred for one hour. Sodium methoxide (28% solution in methanol, 45.73 g, 237 mmol) in methanol (30 ml) was then added to the solution and stirred for 2 hours. Reaction was quenched by adding dilute hydrochloric acid to adjust the pH around 7.0, and partitioned between water and ethyl acetate. The organic layer was washed with dilute hydrochloric acid, water, saturated aqueous sodium bicarbonate, and brine and dried over sodium sulfate. Solvents were removed under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; hexane/ethyl acetate=1/1) to afford 4-benzyl-6-(4-bromo-phenyl)-morpholin-3-one (intermediate 32, 21.26 g, 86%) as a colorless oil.

後処理

  1. stirringstirred for 2 hours
  2. customReaction
  3. customwas quenched
  4. additionby adding dilute hydrochloric acid
  5. custompartitioned between water and ethyl acetate
  6. washThe organic layer was washed with dilute hydrochloric acid, water, saturated aqueous sodium bicarbonate, and brine
  7. dry with materialdried over sodium sulfate
  8. customSolvents were removed under reduced pressure
  9. customthe residue was purified by silica gel column chromatography (eluent; hexane/ethyl acetate=1/1)

出典と根拠

ORDレコード
ord-4c9e41abf45843889c25a2df2227748e
出典データセット
uspto-grants-2012_10
特許番号
US08288383B2

反応ノート

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