HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Salicylaldehyde → HCID 136139912, compound

HRID 1732408
Notes
Print preview

Reaction equation

HRID 1732408 reaction equation
[CH3:1][C:2]1[S:3][C:4]([CH3:7])=[N:5][N:6]=1.[CH:8](=O)[C:9]1[C:10](=[CH:12][CH:13]=[CH:14][CH:15]=1)[OH:11]>>[CH3:1][C:2]1[S:3][C:4]([CH:7]=[CH:8][C:9]2[CH:15]=[CH:14][CH:13]=[CH:12][C:10]=2[OH:11])=[N:5][N:6]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6998SalicylaldehydeHCID 969222,5-Dimethyl-1,3,4-thiadiazole

Product 1

HCID 136139912HCID 136139912, compound

Conditions

Temperature
150 °C

Procedure

570 g (5 moles) of 2,5-dimethyl-1,3,4-thiadiazole and 275 g (2.5 moles) of salicylaldehyde are mixed and the mixture is slowly heated to 150° C. whilst passing nitrogen through it. The mixture is kept at 150° C. for 30 hours and is then cooled, the excess 2,5-dimethyl-1,3,4-thiadiazole is distilled off and the residue is recrystallized from methylglycol. 304 g (56% of theory) of yellow crystals of melting point 253°-254° are obtained.

Workup

  1. temperatureis then cooled
  2. distillationthe excess 2,5-dimethyl-1,3,4-thiadiazole is distilled off
On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes
  • customthe residue is recrystallized from methylglycol
  • custom304 g (56% of theory) of yellow crystals of melting point 253°-254° are obtained
  • Sources & evidence

    ORD record
    ord-fea020733b3d4938a2c5276610f6431d
    Source dataset
    uspto-grants-1980_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04237278

    Reaction notes

    Loading…