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Methylparaben → Methyl 4-[(4-methoxyphenyl)methoxy]benzoate

HRID 990023
ノート
印刷プレビュー

反応式

HRID 990023 の反応式
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.CC(C)([O-])C.[K+].[CH3:18][O:19][C:20]1[CH:27]=[CH:26][C:23]([CH2:24]Cl)=[CH:22][CH:21]=1>CN(C=O)C>[CH3:9][O:8][C:6](=[O:7])[C:5]1[CH:4]=[CH:3][C:2]([O:1][CH2:24][C:23]2[CH:26]=[CH:27][C:20]([O:19][CH3:18])=[CH:21][CH:22]=2)=[CH:11][CH:10]=1
参加物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 7456MethylparabenHCID 699934-Methyloxybenzyl chlorideHCID 23665647Potassium tert-butoxide

生成物 1

HCID 12648420Methyl 4-[(4-methoxyphenyl)methoxy]benzoate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of methyl 4-hydoxybenzoate (6.85 g, 45 mmole) in 80 ml DMF was added potassium tert. butoxide (5.6 g, 51 mmole) and the mixture was stirred at room temperature for one hour. 4-Methoxybenzyl chloride (8.3 g, 52 mmole) was added and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure and 200 ml ethyl acetate was added. The organic phase was washed four times with water, dried with sodium sulfate and evaporated under reduced pressure. Yield: 12.3 g 100%

後処理

  1. stirringthe mixture was stirred overnight at room temperature
  2. customThe mixture was evaporated under reduced pressure and 200 ml ethyl acetate
  3. additionwas added
  4. washThe organic phase was washed four times with water
  5. dry with materialdried with sodium sulfate
  6. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-ada549b18d5d4d8e838eb93ca885be70
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06458772B1

反応ノート

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