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

HRID 709326
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HRID 709326 반응식
[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]
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참가 물질

5

반응물 3

HCID 72132,4-DihydroxybenzaldehydeHCID 8082PiperidineHCID 23665760Sodium Hypochlorite

생성물 1

HCID 147660725-chloro-2,4-dihydroxybenzaldehyde

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

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온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-8842f5f4b7f74785b2d94f2e6fec100e
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09180196B2

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