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2,4-Dihydroxybenzaldehyde → 5-chloro-2,4-dihydroxybenzaldehyde

HRID 1797831
ノート
印刷プレビュー

反応式

HRID 1797831 の反応式
[Cl:1][O-].[Na+].N1CCCCC1.[OH:10][C:11]1[CH:18]=[C:17]([OH:19])[CH:16]=[CH:15][C:12]=1[CH:13]=[O:14]>S(=O)(=O)(O)O>[Cl:1][C:16]1[C:17]([OH:19])=[CH:18][C:11]([OH:10])=[C:12]([CH:15]=1)[CH:13]=[O:14]
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 72132,4-DihydroxybenzaldehydeHCID 8082PiperidineHCID 23665760Sodium Hypochlorite

生成物 1

HCID 147660725-chloro-2,4-dihydroxybenzaldehyde

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

反応条件

温度
0 °C

実験手順

Sodium hypochlorite (75 mL, 0.055 mol) and piperidine (4.68 g, 0.055 mol) were cooled to 0° C., combined cautiously and added dropwise over 2 h to a solution of 2,4,-dihydroxybenzaldehyde (6.91 g, 0.05 mol) in 50% aqueous sulfuric acid (150 mL) while cooling to 0° C. After three additional hours, the precipitate was collected via filtration in quantitative yield. 1H NMR indicates that it is about 65% 5-chloro-2,4-dihdroxybenzaldehyde, with the balance being 3-chloro-2,4-dihdroxybenzaldehyde. The product can be purified via column chromatography and/or repeated recrystallizations from toluene. However, the 3-chloro-2,4-dihdroxybenzaldehyde does not react in the next reaction, so the product was used without further purification.

後処理

  1. filtrationAfter three additional hours, the precipitate was collected via filtration in quantitative yield
  2. customThe product can be purified via column chromatography
  3. customrecrystallizations from toluene
  4. customHowever, the 3-chloro-2,4-dihdroxybenzaldehyde does not react in the next reaction, so the product
  5. customwas used without further purification

出典と根拠

ORDレコード
ord-4cd12ff1a290470ca8ddb4b417eecb09
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08343710B1

反応ノート

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