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Water → 2,4,5-Trichlorophenol

HRID 67805
Notes
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Reaction equation

HRID 67805 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([Cl:9])=[CH:4][C:3]=1[N+]#N.[OH2:12]>>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[C:5]([Cl:9])=[CH:4][C:3]=1[OH:12]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 962WaterHCID 124950682,4,5-Trichlorobenzenediazonium

Product 1

HCID 72712,4,5-Trichlorophenol

Procedure

In the fourth stage, the 2,4,5-trichlorobenzenediazonium strong mineral acid salt in solution in water is hydrolytically decomposed at a temperature from the reflux temperature to a temperature of 375° C. At the lower temperatures, the solution is refluxed in the presence of a cupric salt, the 2,4,5-trichlorophenol formed is steam distilled from the reaction and separately recovered. At higher temperatures of 130° C. to 375° C., preferably from 140° C. to 220° C., the aqueous solution is injected into a column packed with a suitable inert material and maintained at the desired temperature, either with or without additional super-heated steam. The 2,4,5-trichlorophenol steam distills from the top of the heated column and the concentrated aqueous strong mineral acid is recovered from the bottom of the column.

Workup

  1. customis hydrolytically decomposed at a temperature from the reflux temperature to a temperature of 375° C

Sources & evidence

ORD record
ord-2795a14b86a5447da28a5bbfeb9c9230
Source dataset
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04346248

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes