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2-Aminothiophenol → HCID 20566346, compound

HRID 848180
Notes
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Reaction equation

HRID 848180 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[SH:8].[Na].Cl[CH2:11][C:12]1[N:16]=[C:15]([CH2:17]Cl)[O:14][N:13]=1>C(O)C>[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][CH2:11][C:12]1[N:16]=[C:15]([CH2:17][S:8][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[NH2:1])[O:14][N:13]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 87132-AminothiophenolHCID 5360545SodiumHCID 64512061,2,4-Oxadiazole, 3,5-bis(chloromethyl)-

Product 1

HCID 20566346HCID 20566346, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

2-Aminobenzenethiol (5.0 g, 0.04 mol) was dissolved in a solution of sodium (0.92 g, 0.04 mol) in ethanol (50 ml) and 3,5-di(chloromethyl)-1,2,4-oxadiazole (3.3 g, 0.02 mol) was added. After filtration of the mixture, the filtrate was collected and the solvent removed to yield the crude product which on re-crystallisation from isopropanol gave 3,5,-di-(2-aminophenylthiomethyl)-1,2,4-oxadiazole, m.p. 68°.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. additionwas added
  2. filtrationAfter filtration of the mixture
  3. customthe filtrate was collected
  4. customthe solvent removed
  5. customto yield the crude product which
  6. customon re-crystallisation from isopropanol

Sources & evidence

ORD record
ord-5a924ee670364408a20f4cc11a37d940
Source dataset
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04294843

Reaction notes

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