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Hydrogen Sulfide → HCID 58283708, compound

HRID 1096054
Notes
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Reaction equation

HRID 1096054 reaction equation
[SH2:1].[NH2:2][C:3](=[C:8]([C:11]#[N:12])[C:9]#[N:10])[C:4]([CH3:7])([CH3:6])[CH3:5].C(N(CC)CC)C.N1C=CC=CC=1>>[NH2:2]/[C:3](/[C:4]([CH3:7])([CH3:5])[CH3:6])=[C:8](\[C:9]#[N:10])/[C:11](=[S:1])[NH2:12]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 402Hydrogen SulfideHCID 1049PyridineHCID 8471TriethylamineHCID 10236016(1-Amino-2,2-dimethylpropylidene)propanedinitrile

Product 1

HCID 58283708HCID 58283708, compound

Procedure

With cooling, 1.52 g (4.50 mmol) of hydrogen sulphide are introduced as a gas into a mixture of 1.6 g (1.40 mmol) of (1-amino-2,2-dimethylpropylidene)propanedinitrile, 1.41 g (1.40 mmol) of triethylamine and 2.21 g (2.80 mmol) of pyridine. For 1 h, nitrogen is then passed through the reaction mixture, and the reaction mixture is then added to ice-water and extracted with dichloromethane. The combined organic phases are dried over Mg2SO4 and freed from the solvent under reduced pressure.

Workup

  1. temperatureWith cooling
  2. extractionextracted with dichloromethane
  3. dry with materialThe combined organic phases are dried over Mg2SO4

Sources & evidence

ORD record
ord-b3c46bf3511a46c3a49decbc01766d84
Source dataset
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08138211B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes