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2-(2-Chloro-5-(hydroxymethyl)phenyl)ethanol → 4-Chloro-3-(2-hydroxyethyl)benzaldehyde

HRID 1255231
Notes
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Reaction equation

HRID 1255231 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][OH:9])=[CH:4][C:3]=1[CH2:10][CH2:11][OH:12]>C(Cl)Cl.[O-2].[O-2].[Mn+4]>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[O:9])=[CH:4][C:3]=1[CH2:10][CH2:11][OH:12]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 579893372-(2-Chloro-5-(hydroxymethyl)phenyl)ethanol2×

Product 1

HCID 579890474-Chloro-3-(2-hydroxyethyl)benzaldehyde

Reagents, catalysts & solvents 2

HCID 178418406HCID 178418406, compoundCatalystHCID 6344DichloromethaneSolvent

Procedure

Manganese (IV) dioxide (1.00 g) was added to a solution of 2-(2-chloro-5-(hydroxymethyl)phenyl)ethanol [Aromatic Intermediate 1, step b] (0.205 g) in DCM (10 mL), and the resulting suspension was stirred at room temperature overnight. The mixture was then filtered through Celite, washing the filter pad well with DCM. The filtrate and washings were concentrated under reduced pressure to afford the titled compound as a colourless oil. Yield 0.159 g.

Workup

  1. filtrationThe mixture was then filtered through Celite
  2. washwashing the filter pad well with DCM
  3. concentrationThe filtrate and washings were concentrated under reduced pressure

Sources & evidence

ORD record
ord-a956096c8a684d9bba8c50be80cbd65b
Source dataset
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08455483B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes