1,6-Dibromohexane → 1-(6-Bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzene

HRID 1494261ノート

反応式

HRID 1494261 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]([CH3:12])([CH3:11])[CH3:10])[C:4]=1[O:13][CH3:14].C([Li])CCC.[Br:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]Br>O1CCCC1.CCCCCC>[Br:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][C:8]1[CH:7]=[CH:6][C:5]([C:9]([CH3:11])([CH3:10])[CH3:12])=[C:4]([O:13][CH3:14])[C:3]=1[O:2][CH3:1]

参加物

6

反応物 3

HCID 123681,6-DibromohexaneHCID 12950402HCID 12950402、化合物HCID 178418339Butyllithium

生成物 1

HCID 149864411-(6-Bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzene収率 15%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒2 回HCID 8058Hexane溶媒

実験手順

To 27.0 g (0.139 mole) of 1,2-dimethoxy-3-(1,1-dimethylethyl)benzene in 350 mL of anhydrous tetrahydrofuran cooled in an ice-brine bath at -5° was added. 87 mL (0.139 mole) of 1.6M butyl lithium in hexane over 30 minutes. The reaction mixture was stirred at -5° for 3 hours and then at reflux for 1 hour. After cooling in an ice bath, 21.5 mL (0.139 mole) of 1,6-dibromohexane in 75 mL of tetrahydrofuran was added dropwise. The reaction mixture was then stirred at reflux for 17 hours. The solvent was removed under reduced pressure, 50 mL of 3N hydrochloric acid was added and the product was extracted with ether. The extract was washed with sodium bicarbonate solution, dried and concentrated at reduced pressure to an oil. Purification by HPLC using 20% toluene-hexane gave 7.6 g ((15% yield) of 1-(6-bromohexyl)-2,3-dimethoxy-4-(1,1-dimethylethyl)benzene.

後処理

  1. additionwas added
  2. temperatureat reflux for 1 hour
  3. temperatureAfter cooling in an ice bath
  4. stirringThe reaction mixture was then stirred
  5. temperatureat reflux for 17 hours
  6. customThe solvent was removed under reduced pressure, 50 mL of 3N hydrochloric acid
  7. additionwas added
  8. extractionthe product was extracted with ether
  9. washThe extract was washed with sodium bicarbonate solution
  10. customdried
  11. concentrationconcentrated at reduced pressure to an oil
  12. customPurification by HPLC

出典と根拠

ORDレコード
ord-c374b92fbf8045c0b99ec29fd43025a0
出典データセット
uspto-grants-1991_06
特許番号
US05025036

反応ノート

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