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Isobutanol → 4-Bromo-2-(2-methylpropoxy)benzoic acid

HRID 2220407
ノート
印刷プレビュー

反応式

HRID 2220407 の反応式
[H-].[Na+].[CH3:3][CH:4]([CH3:7])[CH2:5][OH:6].[Br:8][C:9]1[CH:17]=[CH:16][C:12]([C:13]([OH:15])=[O:14])=[C:11](F)[CH:10]=1>CN(C)C=O>[Br:8][C:9]1[CH:17]=[CH:16][C:12]([C:13]([OH:15])=[O:14])=[C:11]([O:6][CH2:5][CH:4]([CH3:7])[CH3:3])[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 6560IsobutanolHCID 24758Sodium hydrideHCID 3026814-Bromo-2-fluorobenzoic acid

生成物 1

HCID 248246454-Bromo-2-(2-methylpropoxy)benzoic acid

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

To a suspension of sodium hydride (60% w/w, 20.5 g) in N,N-dimethylformamide (365 ml) was added 2-methyl-1-propanol (48.7 ml) dropwise below 30° C. over 2 hours under nitrogen atmosphere. To the mixture was added 4-bromo-2-fluorobenzoic acid (50.0 g) slowly below 35° C. To the reaction mixture was added N,N-dimethylformamide (600 ml) and the mixture was stirred at room temperature for 4 days. The reaction mixture was partitioned between water (2000 ml) and hexane (1000 ml). The water layer was separated and acidified with 37% hydrochloric acid. The precipitate was collected by filtration, washed with water and dried at 55° C. to give 4-bromo-2-isobutoxybenzoic acid (62.4 g) as a white solid.

後処理

  1. customThe reaction mixture was partitioned between water (2000 ml) and hexane (1000 ml)
  2. customThe water layer was separated
  3. filtrationThe precipitate was collected by filtration
  4. washwashed with water
  5. customdried at 55° C.

出典と根拠

ORDレコード
ord-d24519aaa6464469aff2a413ad942d50
出典データセット
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07417060B2

反応ノート

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