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Hydrochloric Acid → HCID 10243410, compound

HRID 1199376
Notes
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Reaction equation

HRID 1199376 reaction equation
[CH3:1][NH:2][C:3](=[S:18])[NH:4][NH:5][C:6]([C:8]1[CH:17]=[CH:16][C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=1)=O.C([O-])(O)=O.[Na+].Cl>>[CH3:1][N:2]1[C:6]([C:8]2[CH:17]=[CH:16][C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH:9]=2)=[N:5][NH:4][C:3]1=[S:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 10083909HCID 10083909, compound

Product 1

HCID 10243410HCID 10243410, compound

Procedure

4-Methyl-1-(2-naphthoyl) thiosemicarbazide (12.9 g, 4.97×10-2 mole) and 1 molar aqueous NaHCO3 (480 ml, 4.80×10-1 mole) were stirred and warmed to reflux. After refluxing overnight, the reaction was cooled in an ice bath before being acidified by the dropwise addition of concentrated hydrochloric acid (40 ml, 4.8×10-1 mole). The resulting product was collected by filtration and dried by suction. Mp 223°-225° C.

Workup

  1. temperaturewarmed to reflux
  2. temperature
After refluxing overnight
  • temperaturethe reaction was cooled in an ice bath
  • filtrationThe resulting product was collected by filtration
  • customdried by suction
  • Sources & evidence

    ORD record
    ord-1b12929f8af448ef81d4d5717ff3f854
    Source dataset
    uspto-grants-1990_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04900743

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes