Calcium Carbonate → HCID 57319731, compound

HRID 1607482Notes

Reaction equation

HRID 1607482 reaction equation
[ClH:1].Cl.[NH2:3][C:4]1[C:5]([O:14][CH3:15])=[C:6]([Cl:13])[CH:7]=[C:8]([NH2:12])[C:9]=1[O:10][CH3:11].[OH-].[Na+].[C:18](=[O:21])([O-:20])[O-].[Ca+2].Cl[C:24]([O:26][CH2:27][CH2:28][Cl:29])=[O:25].O1[CH2:35][CH2:34]OCC1>>[Cl:1][CH2:34][CH2:35][O:20][C:18]([NH:3][C:4]1[C:5]([O:14][CH3:15])=[C:6]([Cl:13])[CH:7]=[C:8]([NH:12][C:24]([O:26][CH2:27][CH2:28][Cl:29])=[O:25])[C:9]=1[O:10][CH3:11])=[O:21]

Participants

6

Conditions

Temperature
80 °C

Procedure

0.15 mole (41.3 g) of 3,5-diamino-2,4-dimethoxychlorobenzene dihydrochloride obtained in Example 3, followed by 30 ml of 10N sodium hydroxide was added to 200 ml of dioxane. The temperature was raised to the region of 80° C., and then 15 g of calcium carbonate were added. 43 g of β-chloroethyl chloroformate were then introduced with stirring. Upon completion of the addition, heating was maintained at 90° C. for 15 minutes. The inorganic salts were removed from the reaction mixture by filtration. The expected product crystallized slowly upon dilution of the reaction mixture with iced water. Recrystallized from 96° strength ethanol, it melted at 87° C.

Workup

  1. additionUpon completion of the addition
  2. temperatureheating
  3. temperaturewas maintained at 90° C. for 15 minutes
  4. customThe inorganic salts were removed from the reaction mixture by filtration
  5. customThe expected product crystallized slowly upon dilution of the reaction mixture with iced water
  6. customRecrystallized from 96° strength ethanol, it melted at 87° C.

Sources & evidence

ORD record
ord-4e2fd80d2e55423ebe95eb75b47065fe
Source dataset
uspto-grants-1989_09
Patent number
US04865618

Reaction notes

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