Benzoyl Peroxide → 2-Benzyl-5-nitroisoindoline

HRID 639575

반응식

HRID 639575 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH3:11])[C:7]([CH3:10])=[CH:8][CH:9]=1)([O-:3])=[O:2].C1C(=O)N(Br)C(=O)C1.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.C([O-])([O-])=O.[Na+].[Na+].[CH2:44]([NH2:51])[C:45]1[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=1>CC(C)=O.O.C(Cl)(Cl)(Cl)Cl>[CH2:44]([N:51]1[CH2:11][C:6]2[C:7](=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=2)[CH2:10]1)[C:45]1[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=1

참가 물질

9

반응물 5

HCID 7187Benzoyl PeroxideHCID 74404-Nitro-o-xyleneHCID 7504BenzylamineHCID 10340Sodium CarbonateHCID 67184N-bromobutanimide

생성물 1

HCID 120659772-Benzyl-5-nitroisoindoline수율 33%

시약·촉매·용매 3

HCID 180Acetone용매2회HCID 962Water용매HCID 5943Carbon Tetrachloride용매

실험 절차

Part A. A solution of 4-nitro-o-xylene (38.64 g, 255.9 mmol), NBS (91.1 g, 511.8 mmol), benzoyl peroxide (1.239 g, 5.118 mmol), and CCl4 (400 mL) was heated at reflux for 1 day, then at rt for 2 days. The solid was filtered off and washed with CCl4. The filtrate was evaporated to give the crude dibromo product (80 g). A portion of which (20 g) was dissolved in acetone (170 mL) and water (45 mL), then Na2CO3 (43.1 g, 407 mmol) was slowly added, followed by BnNH2 (7.05 mL, 64.6 mmol) in acetone (22 mL). After 10 h, the solution was concentrated to one-fourth its volume, the salt solid was filtered off, and the filtrate was evaporated. The residue was dissolved in EtOAc, washed with water and brine, dried over sodium sulfate, filtered, and evaporated. The residue was purified by column chromatography to provide the corresponding 2-benzyl-5-nitro-2,3-dihydro-1H-isoindole (5.41 g, 33% yield, over 2 steps): 1H NMR (300 MHz, CDCl3) δ 8.11 (d, 1H), 8.04 (s, 1H), 7.48-7.20 (m, 6H), 4.02 (s, 4H), 3.92 (s, 2H).

후처리

  1. temperatureat reflux for 1 day
  2. filtrationThe solid was filtered off
  3. washwashed with CCl4
  4. customThe filtrate was evaporated
  5. customto give the crude dibromo product (80 g)
  6. waitAfter 10 h
  7. concentrationthe solution was concentrated to one-fourth its volume
  8. filtrationthe salt solid was filtered off
  9. customthe filtrate was evaporated
  10. dissolutionThe residue was dissolved in EtOAc
  11. washwashed with water and brine
  12. dry with materialdried over sodium sulfate
  13. filtrationfiltered
  14. customevaporated
  15. customThe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-7a24bad9989f4d6fbc0c0e68abd4d088
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07691846B2

연결된 노트

불러오는 중…