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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905931Generated: October 31, 2026

Dimethylcarbamoyl Chloride → HCID 178484733, compound

https://huagongshe.com/reaction/1905931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylcarbamoyl ChlorideHCID 6598—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178512773HCID 178512773—
SolventAcetonitrileHCID 6342—
ProductHCID 178484733HCID 17848473392.9%

Reaction Steps

A solution of 1,3-bis{[p-(1,1,2,2-tetrafluoroethoxy)benzylidene]amino}guanidine (29.84 g, 0.06 mol), diisopropylethylamine (15.51 g, 0.12 mol) and dimethylcarbamoyl chloride (129.2 g, 0.12 mol) in acetonitrile (200 mL) is stirred at reflux for 22 hours. The reaction mixture is cooled, and the acetonitrile is evaporated under reduced pressure. The residue is dissolved in ethyl acetate (250 mL), and the organic solution is washed with water, saturated NaCl and dried over Na2SO4. The solvent is evaporated under reduced pressure, and the residue is crystallized from benzene-hexanes to give the desired product as a yellow solid, mp 141.5°-143.5° C. in 92.9% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04649148
Source datasetuspto-grants-1987_03
ORD IDord-56080205d6b1433584149585c52b9c9e
Source noteuspto-grants-1987_03