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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703981Generated: November 2, 2026

Cyclohexyl isocyanate → Cyclohexylformamide

https://huagongshe.com/reaction/1703981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl isocyanateHCID 18502—
ReactantIsocyanateHCID 105034—
ReactantHCID 178418361HCID 178418361—
Catalyst1,4-DioxaneHCID 31275—
SolventTriethylamineHCID 8471—
ProductCyclohexylformamideHCID 1301783.5%

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of cyclohexyl isocyanate (1.25 g.; 0.01 mole) in 100 ml. anhydrous 1,4-dioxane containing two drops of anhydrous triethylamine was mixed with 0.5 gram 10% Pd-on-carbon and shaken at a pressure of 50 p.s.i. of hydrogen on a Parr low pressure hydrogenator. The uptake of hydrogen was complete in two hours. Work up, as in Example 1, gave 1.15 g. of colorless oil containing a trace of isocyanate. The product was purified by slurrying the oil with Skellysolve B, chilling at -15° C. and decanting the supernatant from the crystalline formamide. After drying under high vacuum, the weight of title product was 1.06 g. (83.5% yield). The ir, nmr and glc were identical to an authentic sample.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04125724
Source datasetuspto-grants-1978_11
ORD IDord-3525f5417a87431d84a4f5bdb0f30d16
Source noteuspto-grants-1978_11