Hydrochloric Acid → 1-(4-Chlorophenyl)-4,4,4-trifluorobutane-1,3-dione

HRID 369169ノート

反応式

HRID 369169 の反応式
[F:1][C:2]([F:9])([F:8])[C:3]([O:5]CC)=O.C[O-].[Na+].[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([C:20](=[O:22])[CH3:21])=[CH:16][CH:15]=1.Cl>C(OC)(C)(C)C>[F:9][C:2]([F:1])([F:8])[C:3](=[O:5])[CH2:21][C:20]([C:17]1[CH:18]=[CH:19][C:14]([Cl:13])=[CH:15][CH:16]=1)=[O:22]

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 7467P-ChloroacetophenoneHCID 9794Ethyl trifluoroacetateHCID 10942334Sodium Methoxide

生成物 1

HCID 27738321-(4-Chlorophenyl)-4,4,4-trifluorobutane-1,3-dione収率 93.3%

試薬・触媒・溶媒 1

HCID 15413tert-Butyl methyl ether溶媒2 回

実験手順

Ethyl trifluoroacetate (23.52 g, 166 mmol) was dissolved in methyl tert-butyl ether (75 mL). To the stirred solution was added 25 weight % sodium methoxide (40 mL, 177 mmol). Next 4'-chloroacetophenone (23.21 g, 150 mmol) was dissolved in methyl tert-butyl ether (20 mL), and added to the reaction dropwise. After stirring overnight (15.75 hours), 3N HCl (70 mL) was added. The organic layer was collected, washed with brine (75 mL), dried over MgSO4, filtered, and concentrated in vacuo to give a 35.09 g of yellow-orange solid. The solid was recrystallized from isooctane to give 31.96 g (85%) of the dione: mp 66-67° C.

後処理

  1. additionadded to the reaction dropwise
  2. additionwas added
  3. customThe organic layer was collected
  4. washwashed with brine (75 mL)
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-e693ed903b2b4ba6bc55ef4c43944b5a
出典データセット
uspto-grants-2000_10
特許番号
US06136839

反応ノート

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