Bromobenzene → alpha-Phenyl[1,1'-biphenyl]-4-methanol

HRID 2305261

反応式

HRID 2305261 の反応式
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Mg].[C:9]1([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:14]=[CH:13][C:12]([CH:15]=[O:16])=[CH:11][CH:10]=1.[NH4+].[Cl-]>C1COCC1>[C:2]1([CH:15]([C:12]2[CH:13]=[CH:14][C:9]([C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)=[CH:10][CH:11]=2)[OH:16])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

6

実験手順

A mixture of bromobenzene (0.3 mol) in THF (300 ml) was added dropwise to a mixture of magnesium (0.32 mol) in THF (20 ml). The mixture was stirred and refluxed for 1 hour. A mixture of 4-biphenylcarboxaldehyde (0.3 mol) in THF (500 ml) was added dropwise. The mixture was stirred and refluxed for 2 hours, at room temperature overnight, poured out into a saturated NH4Cl solution and extracted with DCM. The organic layer was separated, washed three times, dried, filtered and the solvent was evaporated. The residue was triturated in hexane, filtered off and purified over silica gel on a glass filter (eluent: CH2Cl2 100%). The pure fractions were collected and the solvent was evaporated. The residue was triturated in DIPE, filtered off and dried, yielding 31 g of (±)-α-phenyl(1,1′-biphenyl)-4-methanol (interm. 23).

後処理

  1. temperaturerefluxed for 1 hour
  2. additionwas added dropwise
  3. stirringThe mixture was stirred
  4. extractionextracted with DCM
  5. customThe organic layer was separated
  6. washwashed three times
  7. customdried
  8. filtrationfiltered
  9. customthe solvent was evaporated
  10. customThe residue was triturated in hexane
  11. filtrationfiltered off
  12. custompurified over silica gel on a glass
  13. filtrationfilter (eluent: CH2Cl2 100%)
  14. customThe pure fractions were collected
  15. customthe solvent was evaporated
  16. customThe residue was triturated in DIPE
  17. filtrationfiltered off
  18. customdried

出典と根拠

ORDレコード
ord-e60be3078c484e729af67d107b00b8f3
出典データセット
uspto-grants-2002_08
特許番号
US06440440B1

関連ノート

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