Potassium Carbonate → HCID 86758276, compound

HRID 2188040Notes

Reaction equation

HRID 2188040 reaction equation
Cl.[OH:2][CH:3]1[O:11][C@H:10]([CH2:12][OH:13])[C@@H:8]([OH:9])[C@H:6]([OH:7])[C@H:4]1[NH2:5].[OH-].[Na+].C(=O)([O-])[O-].[K+].[K+].[N:22]([O-])=O.[Na+].[C:26](Cl)(=[O:29])[CH:27]=[CH2:28]>C(Cl)(Cl)Cl>[C:26]([NH:22][NH:5][C@@H:4]1[C@@H:6]([OH:7])[C@H:8]([OH:9])[C@@H:10]([CH2:12][OH:13])[O:11][CH:3]1[OH:2])(=[O:29])[CH:27]=[CH2:28]

Participants

7

Procedure

Another alternative monomer containing a functional group in the form of a hydroxyl group was prepared in the following manner. Glucosamine hydrochloride 10.0 g, (0.0464 moles) was added to 12 ml of 3.8-M sodium hydroxide. Potassium carbonate 0.30 g, (0.0022 moles) and sodium nitrite 0.35 g, (0.0051 moles) were then added and the mixture was stirred until a clear solution was obtained. To the clear solution was added 10-ml chloroform, and the mixture was stirred vigorously while in an ice bath. A solution of acryloyl chloride 4.45g, (4.0 ml; 0.0492 moles) in 5 ml of chloroform was added in 100 microliter portions with alternate additions of 55 μl of 10 N sodium hydroxide (4.95 ml total) with stirring in an ice bath. The stirring was continued for 30 minutes after the additions were complete. The chloroform was removed. The pH was adjusted to 3 followed by 3×10-ml extractions of chloroform to remove acrylic acid. The water solution was stored at ˜4° C. The use of AGA in polymerization is described in Examples 12 and 13.

Workup

  1. additionAnother alternative monomer containing a functional group in the form of a hydroxyl group
  2. customwas prepared in the following manner
  3. customwas obtained
  4. stirringthe mixture was stirred vigorously while in an ice bath
  5. stirringwith stirring in an ice bath
  6. customThe chloroform was removed
  7. extractionfollowed by 3×10-ml extractions of chloroform
  8. customto remove acrylic acid
  9. customwas stored at ˜4° C
  10. customThe use of AGA in polymerization

Sources & evidence

ORD record
ord-91fdf7962b18482a9726f5604cb78912
Source dataset
uspto-grants-2002_06
Patent number
US06410643B1

Reaction notes

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