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Nitric Acid → 3,7-Dimethyl-5-nitrobenzo[d]isoxazole

HRID 873883
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HRID 873883 반응식
[CH3:1][C:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([CH3:11])[C:5]=2[O:4][N:3]=1.[N+:12]([O-])([OH:14])=[O:13]>OS(O)(=O)=O.O>[CH3:1][C:2]1[C:6]2[CH:7]=[C:8]([N+:12]([O-:14])=[O:13])[CH:9]=[C:10]([CH3:11])[C:5]=2[O:4][N:3]=1
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참가 물질

5

반응물 2

HCID 944Nitric AcidHCID 124113243,7-Dimethylbenzisoxazole

생성물 1

HCID 155612543,7-Dimethyl-5-nitrobenzo[d]isoxazole수율 73%

시약·촉매·용매 2

HCID 962Water용매HCID 1118Sulfuric Acid용매

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온도
0 °C

실험 절차

3,7-dimethylbenzo[d]isoxazole (Step 46.4) (2 g, 12.77 mmol) was dissolved in H2SO4 (5 mL), cooled down and stirred at 0° C. HNO3 (0.878 mL, 12.77 mmol) was slowly added and the resulting mixture was stirred at 0° C. for 1 hr. The reaction was diluted with water (60 mL) and extracted three times with CH2Cl2. The combined organic layers were washed with NaHCO3 solution and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The resulting yellow solid was triturated with Et2O, filtrated off, washed with Et2O and dried to afford the title product (1.86 g, 9.29 mmol, 73% yield) as yellow solid. tR: 0.98 min (LC-MS 2); ESI-MS: 193 [M+H]+.

후처리

  1. temperaturecooled down
  2. stirringthe resulting mixture was stirred at 0° C. for 1 hr
  3. extractionextracted three times with CH2Cl2
  4. washThe combined organic layers were washed with NaHCO3 solution and brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe resulting yellow solid was triturated with Et2O
  9. filtrationfiltrated off
  10. washwashed with Et2O
  11. customdried

출처 및 근거

ORD 기록
ord-963bb350aab54975a84f4751c4ba04f5
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08975417B2

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