Calcium nitrate → HCID 131709957, compound

HRID 1580698Notes

Reaction equation

HRID 1580698 reaction equation
[CH2:1]([C:4]1[C:13]2[O:12][C:11]([C:14]3[NH:18][N:17]=[N:16][N:15]=3)=[CH:10][C:9](=[O:19])[C:8]=2[C:7]([O:20][CH2:21][CH2:22][CH:23]([CH3:25])[CH3:24])=[CH:6][CH:5]=1)[CH:2]=[CH2:3].C(=O)(O)[O-:27].[Na+].[N+]([O-])([O-])=[O:32].[Ca+2:35].[N+]([O-])([O-])=[O:37]>O>[CH2:1]([C:4]1[C:13]2[O:12][C:11]([C:14]3[NH:15][N:16]=[N:17][N:18]=3)=[CH:10][C:9](=[O:19])[C:8]=2[C:7]([O:20][CH2:21][CH2:22][CH:23]([CH3:25])[CH3:24])=[CH:6][CH:5]=1)[CH:2]=[CH2:3].[OH2:27].[OH2:32].[OH2:37].[OH2:12].[OH2:12].[Ca:35]

Participants

6

Procedure

5Parts of 5-[8-allyl-5-(3-methylbutoxy)-4-oxo-4H-1-benzopyran-2-yl]tetrazole and 1.29 parts of sodium bicarbonate were mutually dissolved in 200 parts of water. To this stirred solution 1.25 parts of calcium nitrate in 100 parts of water were added. A creamy precipitate was produced. The mixture was cooled and the precipitate was collected. The compound was finely powdered, treated with boiling water, collected and dried in vacuo. 4.8 Parts of 5-[8-allyl-5-(3-methylbutoxy)-4-oxo-4H-1-benzopyran-2-yl]tetrazole as its calcium salt pentahydrate were obtained.

Workup

  1. customA creamy precipitate was produced
  2. temperatureThe mixture was cooled
  3. customthe precipitate was collected
  4. additiontreated with boiling water
  5. customcollected
  6. customdried in vacuo

Sources & evidence

ORD record
ord-cd2a66902b034edb976c73b3c28a4a79
Source dataset
uspto-grants-1976_01
Patent number
US03933844

Reaction notes

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