Hydrochloric Acid → HCID 15341788, compound

HRID 1756186Notes

Reaction equation

HRID 1756186 reaction equation
[OH:1][C:2]1[C:11]([CH2:12][CH:13]=[CH2:14])=[C:10]([OH:15])[CH:9]=[CH:8][C:3]=1[C:4](OC)=[O:5].[CH3:16][NH2:17].[Cl-].[NH4+].Cl>>[OH:1][C:2]1[C:11]([CH2:12][CH:13]=[CH2:14])=[C:10]([OH:15])[CH:9]=[CH:8][C:3]=1[C:4]([NH:17][CH3:16])=[O:5]

Participants

5

Reactant 4

HCID 313Hydrochloric AcidHCID 6329MethylamineHCID 25517Ammonium ChlorideHCID 13019279Methyl 2,4-dihydroxy-3-(prop-2-en-1-yl)benzoate

Product 1

HCID 15341788HCID 15341788, compoundYield 75%

Procedure

The compound of Example 5 (3.5 g) and excess methyl amine (40% aqueous solution) were stirred overnight at 50° C. in the presence of a few crystals of ammonium chloride. The reaction mixture was cooled and neutralized with 10% hydrochloric acid then extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated under vacuum. The crude crystals were dissolved in chloroform and then hexane was added until the product precipitated out of solution. The precipitate was filtered and dried to give the product (2.5 g, 75% yield).

Workup

  1. temperatureThe reaction mixture was cooled
  2. extractionthen extracted with ethyl acetate
  3. dry with materialThe organic layer was dried over magnesium sulfate
  4. concentrationconcentrated under vacuum
  5. dissolutionThe crude crystals were dissolved in chloroform
  6. additionhexane was added until the product
  7. customprecipitated out of solution
  8. filtrationThe precipitate was filtered
  9. customdried

Sources & evidence

ORD record
ord-fee95d69679e4559b820889195eb140d
Source dataset
uspto-grants-1995_08
Patent number
US05439937

Reaction notes

Loading…