Sodium Bicarbonate → HCID 23683788, compound

HRID 2163404Notes

Reaction equation

HRID 2163404 reaction equation
[C:1]([C:4]1[C:31]([OH:32])=[CH:30][CH:29]=[CH:28][C:5]=1[O:6][CH2:7][CH:8]([OH:27])[CH2:9][O:10][C:11]1[C:16]2[C:17](=[O:26])[CH:18]=[C:19]([C:21]([O:23]CC)=[O:22])[O:20][C:15]=2[CH:14]=[CH:13][CH:12]=1)(=[O:3])[CH3:2].C(=O)(O)[O-].[Na+:37]>O>[C:1]([C:4]1[C:31]([OH:32])=[CH:30][CH:29]=[CH:28][C:5]=1[O:6][CH2:7][CH:8]([OH:27])[CH2:9][O:10][C:11]1[C:16]2[C:17](=[O:26])[CH:18]=[C:19]([C:21]([O-:23])=[O:22])[O:20][C:15]=2[CH:14]=[CH:13][CH:12]=1)(=[O:3])[CH3:2].[Na+:37]

Participants

4

Procedure

32.0 parts of ethyl 5-(3-[2-acetyl-3-hydroxyphenoxy]-2-hydroxypropoxy)-4-oxo-4H-1-benzopyran-2-carboxylate were refluxed with a solution of 6.08 parts of sodium bicarbonate in 200 parts of water for eighteen hours. The solution was filtered hot and cooled. The solid obtained was collected by filtration and crystallised from water containing a small quantity of ethanol to give 9.2 parts of sodium 5-(3-[2-acetyl-3-hydroxyphenoxy]-2-hydroxypropoxy)-4-oxo-4H-1-benzopyran-2-carboxylate, m.pt. 178°-180°.

Workup

  1. filtrationThe solution was filtered hot
  2. temperaturecooled
  3. customThe solid obtained
  4. filtrationwas collected by filtration
  5. customcrystallised from water containing a small quantity of ethanol

Sources & evidence

ORD record
ord-ff0bb24c83834ea08262686d07144d45
Source dataset
uspto-grants-1979_01
Patent number
US04133889

Reaction notes

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