Methanol → 4-(2-(diphenylmethoxy)ethyl)-8-hydroxy-3,4-dihydro-2H-1,4-benzoxazine

HRID 2186728노트

반응식

HRID 2186728 반응식
C([O:4][C:5]1[C:14]2[O:13][CH2:12][CH2:11][N:10]([CH2:15][CH2:16][O:17][CH:18]([C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[C:9]=2[CH:8]=[CH:7][CH:6]=1)(=O)C.CO.C(=O)([O-])[O-].[K+].[K+]>C1COCC1>[C:25]1([CH:18]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[O:17][CH2:16][CH2:15][N:10]2[C:9]3[CH:8]=[CH:7][CH:6]=[C:5]([OH:4])[C:14]=3[O:13][CH2:12][CH2:11]2)[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1

참가 물질

5

반응물 3

HCID 887MethanolHCID 11430Potassium CarbonateHCID 224489878-acetoxy-4-(2-(diphenylmethoxy)ethyl)-3,4-dihydro-2H-1,4-benzoxazine

생성물 1

HCID 213498804-(2-(diphenylmethoxy)ethyl)-8-hydroxy-3,4-dihydro-2H-1,4-benzoxazine수율 99.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

8-acetoxy-4-(2-(diphenylmethoxy)ethyl)-3,4-dihydro-2H-1,4-benzoxazine (482 mg) was dissolved in THF (2 ml) and a methanol (10 ml), and anhydrous potassium carbonate (250 mg) was added to the resultant solution, and the mixture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure, and the residue was poured into 5% citric acid, and then extracted with ethyl acetate. The resultant organic layer was washed with water and saturated brine, dried over sodium sulfate, and then concentrated to obtain the colorless oily object compound (429 mg, yield 99%).

후처리

  1. distillationThe solvent was distilled off under reduced pressure
  2. additionthe residue was poured into 5% citric acid
  3. extractionextracted with ethyl acetate
  4. washThe resultant organic layer was washed with water and saturated brine
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-14cb420f5fee40cd9eea772f15b7fbed
출처 데이터셋
uspto-grants-2002_06
특허 번호
US06407096B1

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