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

3,4-Dichloroaniline → HCID 19006421, compound

HRID 261482
Notes
Print preview

Reaction equation

HRID 261482 reaction equation
[Cl:1][C:2]1[CH:14]=[CH:13][CH:12]=[C:11]([Cl:15])[C:3]=1[C:4]([NH:6][C:7](=[S:10])[SH-]C)=[S:5].[Cl:16][C:17]1[CH:18]=[C:19]([CH:21]=[CH:22][C:23]=1[Cl:24])[NH2:20]>C1(C)C=CC=CC=1>[Cl:15][C:11]1[CH:12]=[CH:13][CH:14]=[C:2]([Cl:1])[C:3]=1[C:4]([NH:6][C:7]([NH:20][C:19]1[CH:21]=[CH:22][C:23]([Cl:24])=[C:17]([Cl:16])[CH:18]=1)=[S:10])=[S:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 72573,4-DichloroanilineHCID 178504154HCID 178504154, compound

Product 1

HCID 19006421HCID 19006421, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

3.0 g of N-(2,6-dichlorothiobenzoyl)-S-methyldithiocarbamate and 1.6 g of 3,4-dichloroaniline are dissolved in 25 ml of toluene and subsequently heated while refluxing for 5 hours. The resulting yellow precipitate is worked up in the usual manner. Yield 2.1 g. Melting point 168°-170° C.

Workup

temperature
subsequently heated
  • temperaturewhile refluxing for 5 hours
  • Sources & evidence

    ORD record
    ord-c4a9c85ce4f74bb69a2a53be64022ae3
    Source dataset
    uspto-grants-1979_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04166124

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes