Dichloromethane → HCID 9900695、化合物

HRID 7822

反応式

HRID 7822 の反応式
B(Br)(Br)Br.C(Cl)Cl.[Br:8][C:9]1[C:10](=[O:25])[CH2:11][CH2:12][C:13]2([CH3:24])[C:21]=1[C:20]1[C:15](=[CH:16][C:17]([O:22]C)=[CH:18][CH:19]=1)[CH2:14]2>>[Br:8][C:9]1[C:10](=[O:25])[CH2:11][CH2:12][C:13]2([CH3:24])[C:21]=1[C:20]1[C:15](=[CH:16][C:17]([OH:22])=[CH:18][CH:19]=1)[CH2:14]2

参加物

4

反応物 3

HCID 6344DichloromethaneHCID 25134Boron tribromideHCID 219908604-bromo-7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one

生成物 1

HCID 9900695HCID 9900695、化合物

実験手順

1M BBr3 in CH2Cl2 (0.200 mL, 0.2 mmol) was added to an ice-cold solution of 4-bromo-7-methoxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (10 mg, 0.033 mmol) in CH2CL2 (0.5 mL). The cooling bath was removed and the solution was stirred at room temperature for 30 minutes, then treated with more BBr3 in CH2CL2 (0.5 mL, 0.5 mmol) and stirred at room temperature for an additional 60 minutes. The solution was diluted with EtOAc (10 mL), washed with water (10 mL), 1N HCl (2 mL), and brine (10 ml), dried over MgSO4, filtered, and evaporated under vacuum to an oil. The crude product was purified by preparative layer chromatography on a 0.05×20×20 cm silica gel GF plate, developing with 5% CH3OH in CH2Cl2, to afford 4-bromo-7-hydroxy-9a-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one as a gum.

後処理

  1. customThe cooling bath was removed
  2. additiontreated with more BBr3 in CH2CL2 (0.5 mL, 0.5 mmol)
  3. stirringstirred at room temperature for an additional 60 minutes
  4. additionThe solution was diluted with EtOAc (10 mL)
  5. washwashed with water (10 mL), 1N HCl (2 mL), and brine (10 ml)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated under vacuum to an oil
  9. customThe crude product was purified by preparative layer chromatography on a 0.05×20×20 cm silica gel GF plate

出典と根拠

ORDレコード
ord-e5a1851da29e4f9a858bacb45e92bc64
出典データセット
uspto-grants-2006_08
特許番号
US07087599B2

関連ノート

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