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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249028Generated: October 30, 2026

Ethanol → Dicyclohexylamine

https://huagongshe.com/reaction/1249028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantCarbon DisulfideHCID 6348—
ReactantDicyclohexylamineHCID 7582—
Reactant1-IodopropaneHCID 33643—
Reactant1,2,3,4-Tetrahydro-Beta-Carboline-3-Carboxylic AcidHCID 98285—
ProductDicyclohexylamineHCID 7582—
ProductHCID 13561929HCID 13561929—

Reaction Steps

To a mixture of (3RS)-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (4.32 g), dicyclohexylamine (7.3 g) and 50% ethanol (55 ml) is added dropwise carbon disulfide (1.2 ml). The mixture is stirred at room temperature for 30 minutes, and thereto is added dropwise n-propyl iodide (3.4 g). The mixture is further stirred at room temperature for 10 minutes. The reaction mixture is distilled to remove the solvent. The resulting precipitates are collected by filtration and washed with ether to give dicyclohexylamine salt of the title compound. This product is treated with 10% HCl to give the title compound (4.6 g, 69%) as colorless needles, m.p. 180° C. (decomp.) (recrystallized from ethanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04628057
Source datasetuspto-grants-1986_12
ORD IDord-f6a71cf185dc4000b58f5720dce3a4c2
Source noteuspto-grants-1986_12