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Hydrochloric Acid → 3-(Methylthio)-5-(trifluoromethyl)benzoic acid

HRID 1606759
Notes
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Reaction equation

HRID 1606759 reaction equation
[SH:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:10]=1)[C:5]([OH:7])=[O:6].[OH-].[Na+].[CH3:17]I.Cl>C(O)C>[CH3:17][S:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([C:11]([F:12])([F:13])[F:14])[CH:10]=1)[C:5]([OH:7])=[O:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 6328Methyl iodideHCID 14798Sodium HydroxideHCID 21542284HCID 21542284, compound

Product 1

HCID 214459703-(Methylthio)-5-(trifluoromethyl)benzoic acid

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Procedure

To a solution of 10 g. (0.045 mole) of 3-mercapto-5-trifluoromethylbenzoic acid, and 100 ml. of 1N sodium hydroxide in 100 ml. of ethanol is added 3.8 ml. (0.06 mole) of methyl iodide. After the reaction has stirred at room temperature for one hour, it is acidified with 12N hydrochloric acid, and the precipitate of the final product is filtered and dried,8.6 g., m.p. 135°-140° C. A sample is sublimed at 175° C. and 0.03 mm pressure, m.p. 151°-152.5° C.

Workup

  1. filtrationthe precipitate of the final product is filtered
  2. customdried
  3. customis sublimed at 175° C.

Sources & evidence

ORD record
ord-6ccdc6fdae374e30a10ed670f7e67ae9
Source dataset
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03953595

Reaction notes

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