4-Chlorobenzaldehyde → HCID 178504058, compound

HRID 267322Notes

Reaction equation

HRID 267322 reaction equation
Br[C:2]1[CH:14]=[CH:13][C:5]([CH:6]=[N:7][NH:8][C:9](=[NH:12])[S:10][CH3:11])=[CH:4][CH:3]=1.[Cl:15]C1C=CC(C=O)=CC=1.C(=N)(SC)NN.C(C1C=CC(C=O)=CC=1)#N.I.C(=N)(SCC)NN.Br.[Cl:49]C1C=C(C=CC=1Cl)C=NNC(=N)SCCC.ClC1C=C(C=CC=1Cl)C=O.Br.C(=N)(SCCC)NN>>[ClH:15].[Cl:49][C:2]1[CH:14]=[CH:13][C:5]([CH:6]=[N:7][NH:8][C:9](=[NH:12])[S:10][CH3:11])=[CH:4][CH:3]=1

Participants

9

Reactant 8

HCID 77264-ChlorobenzaldehydeHCID 227103,4-DichlorobenzaldehydeHCID 660424-CyanobenzaldehydeHCID 178419558HCID 178419558, compoundHCID 178419559HCID 178419559, compoundHCID 178477489HCID 178477489, compoundHCID 178504051Methyl hydrazinecarbimidothioateHCID 178504057HCID 178504057, compound

Product 1

HCID 178504058HCID 178504058, compound

Procedure

The following are prepared in like manner: methyl 3-(4-bromobenzylidene)thiocarbazimidate methosulfate from 4-chlorobenzaldehyde and methyl thiocarbazimidate methosulfate, ethyl 3-(4-cyanobenzylidine)thiocarbazimidate hydroiodide from 4-cyanobenzaldehyde and ethyl thiocarbazimidate hydroiodide, and propyl 3-(3,4-dichlorobenzylidene)thiocarbazimidate hydrobromide from 3,4-dichlorobenzaldehyde and propyl thiocarbazimidate hydrobromide.

Workup

  1. customThe following are prepared in like manner

Sources & evidence

ORD record
ord-02088281e21a43ab8944a99d0e44aef2
Source dataset
uspto-grants-1976_03
Patent number
US03941825

Reaction notes

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