Dichloromethane → 7-tert-Butyl-1-methylpyrene

HRID 1914410ノート

反応式

HRID 1914410 の反応式
[CH3:1][C:2]1[C:15]2[C:16]3=[C:17]4[C:12](=[CH:13][CH:14]=2)[CH:11]=[CH:10][CH:9]=[C:8]4[CH:7]=[CH:6][C:5]3=[CH:4][CH:3]=1.[C:18](Cl)([CH3:21])([CH3:20])[CH3:19].ClCCl.[Cl-].[Al+3].[Cl-].[Cl-]>O>[C:18]([C:10]1[CH:9]=[C:8]2[C:17]3=[C:16]4[C:5](=[CH:4][CH:3]=[C:2]([CH3:1])[C:15]4=[CH:14][CH:13]=[C:12]3[CH:11]=1)[CH:6]=[CH:7]2)([CH3:21])([CH3:20])[CH3:19]

参加物

6

反応物 4

HCID 6344DichloromethaneHCID 10486tert-BUTYL CHLORIDEHCID 169321-MethylpyreneHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 30866837-tert-Butyl-1-methylpyrene収率 54.1%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Next, a mixed solution of 4.4 g of 1-methylpyrene, 2 g of t-butylchloride and 33 ml of dichloromethane was cooled to 0° C. under a nitrogen gas stream and then 2.7 g of aluminum chloride was added. This mixed solution was stirred at room temperature for 3 hours and 30 ml of water was poured into the solution, followed by extraction with 30 ml of dichloromethane. The organic layer was washed twice with 20 ml of water, dried over magnesium sulfate and then evaporated. The concentrate was purified by silica gel column chromatography and then vacuum-dried to obtain 3 g of 7-t-butyl-1-methylpyrene.

後処理

  1. extractionfollowed by extraction with 30 ml of dichloromethane
  2. washThe organic layer was washed twice with 20 ml of water
  3. dry with materialdried over magnesium sulfate
  4. customevaporated
  5. customThe concentrate was purified by silica gel column chromatography
  6. customvacuum-dried

出典と根拠

ORDレコード
ord-ae6368f67b7047a489bc72fcffdf2610
出典データセット
uspto-grants-2013_12
特許番号
US08610345B2

反応ノート

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