HCID 22417270, compound → HCID 22417281, compound

HRID 487817Notes

Reaction equation

HRID 487817 reaction equation
[CH3:1][C:2]([N:5]1[N:9]=[N:8][C:7]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([CH2:17][CH2:18][C:19]([O:21]C(C)(C)C)=[O:20])=[CH:13][CH:12]=2)=[N:6]1)([CH3:4])[CH3:3]>FC(F)(F)C(O)=O>[CH3:4][C:2]([N:5]1[N:9]=[N:8][C:7]([CH2:10][C:11]2[CH:12]=[CH:13][C:14]([CH2:17][CH2:18][C:19]([OH:21])=[O:20])=[CH:15][CH:16]=2)=[N:6]1)([CH3:1])[CH3:3]

Participants

3

Reactant 1

HCID 22417270HCID 22417270, compound

Product 1

HCID 22417281HCID 22417281, compoundYield 66%

Reagents, catalysts & solvents 1

HCID 6422Trifluoroacetic acidSolvent

Procedure

1,1-dimethylethyl 4-[[2-(1,1-dimethylethyl)-2H-tetrazol-5-yl]methyl]benzenepropanoate (3.0 g. 8.7 mmol) was dissolved in trifluoroacetic acid (33 mL) and stirred at room temperature under argon for 12 hours. The mixture was concentrated and then dissolved in water (50 ml). After adding enough sat. NaHCO3 to raise the pH to 8, the solution was washed with diethyl ether (2×25 mL). The aqueous layer was acidified to pH 3 with 1N HCl and the product collected by suction filtration. Recrystallization from hexanes gave 4-[[2-(1,1-dimethylethyl)-2H-tetrazol-5-yl]methyl]benzene-propanoic acid (1.5 g, 5.7 mmol) in 66% yield, mp. 139°-141° C.

Workup

  1. concentrationThe mixture was concentrated
  2. dissolutiondissolved in water (50 ml)
  3. additionAfter adding enough sat. NaHCO3
  4. temperatureto raise the pH to 8
  5. washthe solution was washed with diethyl ether (2×25 mL)
  6. filtrationthe product collected by suction filtration
  7. customRecrystallization from hexanes

Sources & evidence

ORD record
ord-ccbb7dd55c6c4ac3b123d5381484cf88
Source dataset
uspto-grants-1994_03
Patent number
US05296608

Reaction notes

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