Sulfuric Acid → (3-Benzyloxy-5-trifluoromethylthien-2-yl)-carboxylic acid

HRID 1422178Notes

Reaction equation

HRID 1422178 reaction equation
[CH2:1]([O:8][C:9]1[CH:13]=[C:12]([C:14]([F:17])([F:16])[F:15])[S:11][C:10]=1[C:18]([O:20]C)=[O:19])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O1CCCC1.S(=O)(=O)(O)O>[OH-].[Na+]>[CH2:1]([O:8][C:9]1[CH:13]=[C:12]([C:14]([F:15])([F:16])[F:17])[S:11][C:10]=1[C:18]([OH:20])=[O:19])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

5

Reactant 3

HCID 1118Sulfuric AcidHCID 8028TetrahydrofuranHCID 11278508Methyl (3-benzyloxy-5-trifluoromethylthien-2-yl)-carboxylate

Product 1

HCID 11426602(3-Benzyloxy-5-trifluoromethylthien-2-yl)-carboxylic acidYield 89%

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent

Procedure

A mixture of 1E (3.80 g) and tetrahydrofuran (12 ml) was heated to reflux in 2N sodium hydroxide (12 ml) for 12 hours. Then the mixture was poured on ice and acidified with 6N sulfuric acid (pH=1-2). The mixture is extracted with diethyl ether twice. The combined organic phases were washed with water and dried. The mixture was concentrated and the residue is distilled under reduced pressure to yield the product as a white solid (3.22 g, 89%) with a melting point of 142-144° C.

Workup

  1. temperaturewas heated
  2. additionThen the mixture was poured on ice
  3. extractionThe mixture is extracted with diethyl ether twice
  4. washThe combined organic phases were washed with water
  5. customdried
  6. concentrationThe mixture was concentrated
  7. distillationthe residue is distilled under reduced pressure

Sources & evidence

ORD record
ord-1198d70bbd734d2095212405bf15800a
Source dataset
uspto-grants-2000_06
Patent number
US06080861

Reaction notes

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