Hydrochloric Acid → 2-Chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylic acid

HRID 1903662Notes

Reaction equation

HRID 1903662 reaction equation
[Cl:1][C:2]1[S:3][C:4]([C:11]([O:13]CC)=[O:12])=[C:5]([C:7]([F:10])([F:9])[F:8])[N:6]=1.[OH-].[Na+].O.Cl>O1CCCC1>[Cl:1][C:2]1[S:3][C:4]([C:11]([OH:13])=[O:12])=[C:5]([C:7]([F:9])([F:8])[F:10])[N:6]=1

Participants

6

Procedure

A mixture of 116 g (0.4468 mole) of ethyl 2-chloro-4-trifluoromethyl-5-thiazolecarboxylate, 18 g (0.45 mole) of sodium hydroxide, 200 ml. of water, 400 ml. of tetrahydrofuran was stirred at room temperature for 16 hours and made acidic with 50 ml. of concentrated hydrochloric acid. The reaction mixture was extracted twice with 200 ml. of ether. The ether-tetrahydrofuran solution was dried (MgSO4) and concentrated under reduced pressure. The residual oil was treated with benzene and the benzene solution was concentrated under reduced pressure to remove the last trace of water. The residual solid was recrystallized from hexane-benzene to give 76 g (73.4%) of 2-chloro-4-trifluoromethyl-5-thiazolecarboxylic acid, m.p. 131°-131.5° C.

Workup

  1. extractionThe reaction mixture was extracted twice with 200 ml
  2. dry with materialThe ether-tetrahydrofuran solution was dried (MgSO4)
  3. concentrationconcentrated under reduced pressure
  4. additionThe residual oil was treated with benzene
  5. concentrationthe benzene solution was concentrated under reduced pressure
  6. customto remove the last trace of water
  7. customThe residual solid was recrystallized from hexane-benzene

Sources & evidence

ORD record
ord-28cbb2610cfc47dc831f0c9da5261a45
Source dataset
uspto-grants-1984_03
Patent number
US04437875

Reaction notes

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