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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614016Generated: October 30, 2026

Cyanide → HCID 21329854, compound

https://huagongshe.com/reaction/614016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanideHCID 5975—
ReactantN-MethylanilineHCID 7515—
Reactant1,2-Dichloro-4-(2-isocyanatopropan-2-yl)benzeneHCID 21329862—
SolventBenzeneHCID 241—
ProductHCID 21329854HCID 2132985486%

Reaction Steps

4.6 g of 3,4-dichloro-α,α-dimethylbenzyl isocyanate, prepared from the corresponding cyanide in the same way as in Synthesis Example 1, was added to a solution of 2.2 g of N-methylaniline in 20 ml of benzene and the mixture was heated under reflux for 2 hours. After allowing the mixture to stand overnight, the reaction solution was washed with a 2N aqueous hydrochloric acid solution, a 2N aqueous sodium hydroxide solution and water in that order, and the organic layer was dried over sodium sulfate. The layer was concentrated by evaporating off the solvent to obtain crystals, which were recrystallized from n-hexane to obtain 5.8 g of the title compound as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04143061
Source datasetuspto-grants-1979_03
ORD IDord-64fb70389af14900afa269db32f35d9d
Source noteuspto-grants-1979_03