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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614015Generated: October 27, 2026

Cyanide → 3-(m-Chloro-alpha,alpha-dimethylbenzyl)-1-cyclohexyl-1-methylurea

https://huagongshe.com/reaction/614015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanideHCID 5975—
ReactantN-MethylcyclohexylamineHCID 7514—
Reactant1-Chloro-3-(2-isocyanatopropan-2-yl)benzeneHCID 21329849—
SolventBenzeneHCID 241—
SolventHexaneHCID 8058—
Product3-(m-Chloro-alpha,alpha-dimethylbenzyl)-1-cyclohexyl-1-methylureaHCID 2132983990.7%

Reaction Steps

A solution of 1.2 g of N-methyl-N-cyclohexylamine in 5 ml of n-hexane was added to a solution of 0.01 mole of m-chloro-α,α-dimethylbenzyl isocyanate (prepared from the corresponding cyanide in the same way as shown in Synthesis Example 1) in 10 ml of benzene. The mixture was kept at room temperature for 6 hours and concentrated under reduced pressure to obtain crystals, which were recrystallized from n-hexane to give 2.8 g of the title compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04143061
Source datasetuspto-grants-1979_03
ORD IDord-38dc2c6bcd744c38b6d1f74a83f09570
Source noteuspto-grants-1979_03