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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726506Generated: November 3, 2026

Cyclohexylamine → HCID 24319741, compound

https://huagongshe.com/reaction/1726506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantTriethylamineHCID 8471—
Reactant4-methylnaphthalene-1-sulfonyl ChlorideHCID 2800760—
SolventDichloromethaneHCID 6344—
ProductHCID 24319741HCID 2431974166.1%

Reaction Steps

To a solution of 4-methyl-naphthalene -1-sulfonyl chloride (2.4 g, 10.0 mnmol) in CH2Cl2 (30 mL), was added cyclohexylamine (1.4 g, 11.0 mmol) and triethylamine (2.8 mL, 20.0 mmol) and the resultant solution was stirred at room temperature overnight. The solution was quenched with water and extracted with CH2Cl2 (3×30 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The resulting residue was purified by Flash columin chromatography (hexane/ethyl acetate, gradient elution) to give the title compound 40 (2.0 g) as a yellow solid. 1H NMR (300 MHz, CDCl3) δ 8.63 (d, 1H), 8.18 (d, 1H1), 8.10 (d, 1H1), 7.64 (m, 2H), 7.38 (d, 1H), 3.08 (m, 1H), 2.76 (s, 3H), 1.52 (m, 5H), 1.09 (m, 5H); LC/MS m/z 304 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491827B2
Source datasetuspto-grants-2009_02
ORD IDord-16ed541e387c440c92c2d09c194bf147
Source noteuspto-grants-2009_02