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Resorcinol → 3,5-Di-tert-butyl-2',4,4'-trihydroxybenzophenone

HRID 1885510
ノート
印刷プレビュー

反応式

HRID 1885510 の反応式
[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])[C:8](Cl)=[O:9])([CH3:4])([CH3:3])[CH3:2].[C:19]1([CH:26]=[CH:25][CH:24]=[C:22]([OH:23])[CH:21]=1)[OH:20].[Cl-].[Al+3].[Cl-].[Cl-]>[N+](C1C=CC=CC=1)([O-])=O>[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])[C:8]([C:24]1[CH:25]=[CH:26][C:19]([OH:20])=[CH:21][C:22]=1[OH:23])=[O:9])([CH3:4])([CH3:3])[CH3:2]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 5054ResorcinolHCID 37871873,5-Di-tert-butyl-4-hydroxybenzoyl chlorideHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 197339413,5-Di-tert-butyl-2',4,4'-trihydroxybenzophenone収率 90.8%

試薬・触媒・溶媒 1

HCID 7416Nitrobenzene溶媒

反応条件

温度
50 °C

実験手順

107.5 g of 3,5-di-tert-butyl-4-hydroxybenzoyl chloride and 48.4 g of resorcinol are suspended in 400 ml of nitrobenzene and warmed to 50° C. The brown solution is cooled to 0° C. 58.7 g of aluminium chloride are added in portions over the course of 45 minutes with vigorous stirring. The reaction mixture is slowly warmed to 20° C. over the course of 18 hours. The mixture is subsequently stirred at 50° C. for a further 4 hours, then cooled to room temperature and poured into 500 ml of hydrochloric acid/ice. The thick yellow suspension is extracted with ether, the ether phase is extracted with 500 ml of sodium hydroxide (15%), and the basic solution is washed three times with 250 ml of ether in each case, acidified to a pH of 1-2 using 15% hydrochloric acid and extracted with ether. The ether extracts are combined, dried and evaporated under reduced pressure, giving 124.4 g of 3,5-di-tert-butyl-2',4,4'-trihydroxybenzophenone, which, after recrystallisation from methanol, has a melting point of 192°-193° C.

後処理

  1. temperatureThe brown solution is cooled to 0° C
  2. temperatureThe reaction mixture is slowly warmed to 20° C. over the course of 18 hours
  3. temperaturecooled to room temperature
  4. extractionThe thick yellow suspension is extracted with ether
  5. extractionthe ether phase is extracted with 500 ml of sodium hydroxide (15%)
  6. washthe basic solution is washed three times with 250 ml of ether in each case
  7. extractionextracted with ether
  8. customdried
  9. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-469c605f0ab34c91b6ad2b40fff676c0
出典データセット
uspto-grants-1992_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05145766

反応ノート

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