4-Bromotoluene → 6-Bromo-1,1-dimethyl-4-p-tolyl-1,2-dihydronaphthalene

HRID 2604

반응식

HRID 2604 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.[CH3:9][C:10]1([CH3:22])[C:19]2[C:14](=[CH:15][C:16]([Br:20])=[CH:17][CH:18]=2)[C:13](=O)[CH2:12][CH2:11]1>C1COCC1.C(OC(=O)C)C>[C:5]1([CH3:8])[CH:6]=[CH:7][C:2]([C:13]2[C:14]3[C:19](=[CH:18][CH:17]=[C:16]([Br:20])[CH:15]=3)[C:10]([CH3:22])([CH3:9])[CH2:11][CH:12]=2)=[CH:3][CH:4]=1

참가 물질

5

반응물 2

HCID 78054-BromotolueneHCID 107533577-Bromo-4,4-dimethyl-1,2,3,4-tetrahydronaphthalen-1-one2회

생성물 1

HCID 106876226-Bromo-1,1-dimethyl-4-p-tolyl-1,2-dihydronaphthalene

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매4회HCID 8857Ethyl Acetate용매

실험 절차

To a mixture of Mg metal (650 mg, 27 mmol) in THF (20 mL) was added 4-bromotoluene (5.3 g, 31 mmol) in THF (40 mL). The mixture was stirred for 2 hours at ambient temperature and heated to 70° C. for 30 minutes. After cooling to ambient temperature, 3,4-dihydro-4,4-dimethyl-7-bromo-1(2H)-naphthalenone (Compound A) (2.1 g, 8 mmol), in THF (5 mL) was added and heated to 70° C. for 24 hours. The mixture was cooled to ambient temperature and the reaction was quenched by addition of H2O. The mixture was diluted with ether:ethylacetate (1:1, 100 mL) and washed with saturated NH4Cl (15 mL), water (10 mL) and brine (10 mL). The organic layer was dried with MgSO4. Solvent was removed under reduced pressure to afford the crude product as an off. The product was dissolved in THF (20 mL). To this solution p-toleune sulfonic acid (pTSA) (35 mg) was added and the mixture was refluxed for 16 hours. The mixture was cooled to ambient temperature, diluted with ethylacetate (160 mL), washed with 10% NaHCO3 (20 mL), brine (20 mL), dried with MgSO4 and the solvent wasremoved by evaporation. Purification by chromatography on silica gel gave the title compound as a white solid.

후처리

  1. temperatureheated to 70° C. for 30 minutes
  2. temperatureAfter cooling to ambient temperature
  3. temperatureheated to 70° C. for 24 hours
  4. temperatureThe mixture was cooled to ambient temperature
  5. customthe reaction was quenched by addition of H2O
  6. additionThe mixture was diluted with ether:ethylacetate (1:1, 100 mL)
  7. washwashed with saturated NH4Cl (15 mL), water (10 mL) and brine (10 mL)
  8. dry with materialThe organic layer was dried with MgSO4
  9. customSolvent was removed under reduced pressure
  10. customto afford the crude product as an off
  11. temperaturethe mixture was refluxed for 16 hours
  12. temperatureThe mixture was cooled to ambient temperature
  13. washwashed with 10% NaHCO3 (20 mL), brine (20 mL)
  14. dry with materialdried with MgSO4
  15. customthe solvent wasremoved by evaporation
  16. customPurification by chromatography on silica gel

출처 및 근거

ORD 기록
ord-98343e58e325465bbbaa7fdb2b6a1ac0
출처 데이터셋
uspto-grants-1998_03
특허 번호
US05728846

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