Hydrochloric Acid → HCID 178493933, compound

HRID 1461706Notes

Reaction equation

HRID 1461706 reaction equation
C[O-].[Na+].[CH3:4][O:5][CH:6]([C:11]([O:13]C)=O)[C:7](OC)=[O:8].C(O)(=O)C.[CH:19]([NH2:21])=[NH:20].Cl>CO>[OH:13][C:11]1[C:6]([O:5][CH3:4])=[C:7]([OH:8])[N:21]=[CH:19][N:20]=1

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 78718Dimethyl methoxymalonateHCID 160693Formamidine acetateHCID 10942334Sodium Methoxide

Product 1

HCID 178493933HCID 178493933, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A modified procedure of Bretschneider, Richter, and Klotzer, Monatsh. Chem. 96(6), 1661-76 (1965), was used. Absolute methanol (1.0 l) was added with ice bath cooling to sodium methoxide (175 g, 3.24 mole) in a 3 L round bottom flask. When the mixture had cooled to less than 20° C., dimethyl methoxymalonate (162.14 g, 1.00 mole) was added, and then solid formamidine acetate (104.11 g, 1.00 mole) was added. The mixture was stirred in the ice bath for 30 minutes, and then refluxed for 1 hour. The mixture was cooled in a cold water bath and then concentrated HCl (about 350 mL) was added until the mixture was strongly acidic on pH test paper. The precipitate was filtered, suspended in cold water (about 400 ml), and then filtered again. The white powder was dried in vacuo (125.84 g, 88.7%), and carried on without further purification.

Workup

  1. temperatureWhen the mixture had cooled to less than 20° C.
  2. temperaturerefluxed for 1 hour
  3. temperatureThe mixture was cooled in a cold water bath
  4. filtrationThe precipitate was filtered
  5. filtrationfiltered again
  6. customThe white powder was dried in vacuo (125.84 g, 88.7%)
  7. customcarried on without further purification

Sources & evidence

ORD record
ord-8248377f1a574113afddd036f458858f
Source dataset
uspto-grants-1991_12
Patent number
US05077293

Reaction notes

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