HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28063Generated: October 28, 2026
Acetonitrile → HCID 178464561, compound
https://huagongshe.com/reaction/28063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | HCID 178464630 | HCID 178464630 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178464561 | HCID 178464561 | — |
Reaction Steps
To a magnetically stirred stined suspension of 10/5 g (40 mmol) of 1-(2',6'-diethylphenyl)-3-ethylamidinourea in 10 ml of CH3CN is added 9.52 g (80 mmol) of N,N-dimethylformamide dimethylacetal and another 20 ml of CH3CN. The reaction mixture is heated to reflux at which point all of the solid dissolves. The solution is refluxed for one hour, allowed to cool to ambient temperature and then concentrated in vacuo to yield an off-white solid which is taken up in CHCl3, washed with H2O) (2×50 ml) and saturated aqueous brine (2×25 ml). All aqueous wash layers are combined and back-extracted with CHCl3, (2×25 ml). All organic layers are combined, dried (Na2SO2), filtered and the filtrate concentrated in vacuo to yield a yellow oil. The oil is taken up in MeOH and acidified with HCl/MeOH then concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04225315 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-4604028e153449e28076f7f62bacf13c |
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| Source note | uspto-grants-1980_09 |
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