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Hydrochloric Acid → 7-benzenesulfonyl-3,4-dihydro-2H-benzo[1,4]oxazine

HRID 2224056
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HRID 2224056 반응식
[C:1]1([S:7]([C:10]2[CH:20]=[CH:19][C:13]3[NH:14][C:15](=O)[CH2:16][O:17][C:12]=3[CH:11]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.O.C(=O)([O-])[O-].[K+].[K+]>C1COCC1>[C:1]1([S:7]([C:10]2[CH:20]=[CH:19][C:13]3[NH:14][CH2:15][CH2:16][O:17][C:12]=3[CH:11]=2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 11430Potassium CarbonateHCID 586415157-benzenesulfonyl-4H-benzo[1,4]oxazin-3-one

생성물 1

HCID 586415137-benzenesulfonyl-3,4-dihydro-2H-benzo[1,4]oxazine수율 79.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

실험 절차

A suspension of 7-benzenesulfonyl-4H-benzo[1,4]oxazin-3-one (2.314 g., 8.00 mmol) in 30 ml anhydrous THF was brought to reflux, and borane-dimethyl sulfide complex (2.4 mL, 10 M solution) was added dropwise via syringe. The solution was refluxed for two hours, at which time the solution was cooled to room temperature and ethanolic HCl (10 mL., 2 N solution) was added dropwise. The resulting solution was refluxed for 3 hours and allowed to cool to room temperature. The reaction mixture was poured into 100 mL water, the resulting solution made basic with potassium carbonate and extracted three times with 50 mL Et2O. The organic fractions were washed with 100 mL brine, dried over Na2SO4 and concentrated in vacuo. The resulting residue was purified by flash chromatography (20 to 50% EtOAc in hexanes) to give 1.75 g of 7-benzenesulfonyl-3,4-dihydro-2H-benzo[1,4]oxazine (79.5%) as a yellow solid. MS: 276 (M+H)+.

후처리

  1. temperatureto reflux
  2. additionborane-dimethyl sulfide complex (2.4 mL, 10 M solution) was added dropwise via syringe
  3. temperatureThe solution was refluxed for two hours, at which time the solution
  4. temperatureThe resulting solution was refluxed for 3 hours
  5. temperatureto cool to room temperature
  6. extractionextracted three times with 50 mL Et2O
  7. washThe organic fractions were washed with 100 mL brine
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated in vacuo
  10. customThe resulting residue was purified by flash chromatography (20 to 50% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-d782737fc5bf4216992b05230f1594fb
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07378415B2

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