Diisopropylaniline → Propylbenzene

HRID 370294

反応式

HRID 370294 の反応式
F[C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]([C:12]2C=CC(F)=CC=2)=O)=O)=[CH:4][CH:3]=1.C(C1C=CC=C(C(C)C)C=1N)(C)C>[Ti](Cl)(Cl)(Cl)Cl.C1C=CC=CC=1>[CH2:8]([C:5]1[CH:6]=[CH:7][CH:2]=[CH:3][CH:4]=1)[CH2:10][CH3:12]

参加物

5

反応条件

温度
2 °C

実験手順

In a 250--mL RB flask fitted with pressure equalizing addition funnel, thermometer, magnetic stirrer, and N2 inlet was placed 0.75 g (3.0 mmol) of 4,4'-difluorobenzil, 13.8 mL (80 mmol) of 2,6-diisopropylaniline (DIPA), and 100 mL dry benzene. In the addition funnel was placed 50 mL of dry benzene and 210 mL (3.5 g; 18 mmol) of titanium tetrachloride. The reaction flask was cooled to 2° C. with ice and the TiCl4 solution was added dropwise over 45 min, keeping the reaction temperature below 5° C. The ice bath was removed after addition was complete and the mixture was stirred at RT for 72 h. The reaction mixture was partitioned between water and ethyl ether, and the ether phase was rotovapped and the concentrated oil was washed with 800 mL 1N HCl to remove the excess diisopropylaniline. The mixture was extracted with 100 mL of ether, and the ether layer was washed with water and rotovapped. Addition of 15 mL hexane plus 30 mL of methanol to the concentrate resulted in the formation of fine yellow crystals which were filtered, methanol-washed, and dried under suction to yield 0.4 g of (2,6--i--PrPh)2DAB(4--F--Ph)2, mp: 155°-158° C.

後処理

  1. customIn a 250--mL RB flask fitted with pressure
  2. additionaddition funnel
  3. customthermometer, magnetic stirrer, and N2 inlet was placed
  4. customthe reaction temperature below 5° C
  5. customThe ice bath was removed
  6. additionafter addition
  7. customThe reaction mixture was partitioned between water and ethyl ether
  8. washthe concentrated oil was washed with 800 mL 1N HCl
  9. customto remove the excess diisopropylaniline
  10. extractionThe mixture was extracted with 100 mL of ether
  11. washthe ether layer was washed with water
  12. additionAddition of 15 mL hexane plus 30 mL of methanol to the concentrate
  13. customresulted in the formation of fine yellow crystals which
  14. filtrationwere filtered
  15. washmethanol-washed
  16. customdried under suction

出典と根拠

ORDレコード
ord-f6a9810ca5a34be3a064857afd9b7fe0
出典データセット
uspto-grants-2000_10
特許番号
US06140439

関連ノート

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