Sodium Hydroxide → (+/-)-5decyl-alpha-phenyl-2H-tetrazole-2-acetic acid

HRID 2380474Notes

Reaction equation

HRID 2380474 reaction equation
[OH-].[Na+].[CH2:3]([C:13]1[N:14]=[N:15][N:16]([CH:18]([C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=2)[C:19]([O:21]CC)=[O:20])[N:17]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]>C(O)C>[CH2:3]([C:13]1[N:14]=[N:15][N:16]([CH:18]([C:24]2[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=2)[C:19]([OH:21])=[O:20])[N:17]=1)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Participants

4

Procedure

Solid NaOH (0.33 g, 0.0084 mol) was added to a solution of ethyl (±)-5-decyl-α-phenyl-2H-tetrazole-2-acetate in 50 mL ethanol (90%). The resulting solution was stirred for 1 hour and concentrated in vacuo. The residue was partitioned between diethyl ether and water and the aqueous layer was acidified with 1N HCl. The acidified aqueous layer was extracted with diethyl ether and this ether layer was dried over MgSO4, filtered, and evaporated to give the title compound (1.78 g, 92%), mp 62°-64° C.

Workup

  1. concentrationconcentrated in vacuo
  2. customThe residue was partitioned between diethyl ether and water
  3. extractionThe acidified aqueous layer was extracted with diethyl ether
  4. dry with materialthis ether layer was dried over MgSO4
  5. filtrationfiltered
  6. customevaporated

Sources & evidence

ORD record
ord-8383250a87524357bae4c587952e8378
Source dataset
uspto-grants-1994_11
Patent number
US05366987

Reaction notes

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