Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239217Generated: November 2, 2026

Hydrochloric Acid → HCID 59304065, compound

https://huagongshe.com/reaction/2239217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3-(Dimethylamino)benzoic acidHCID 66837—
ReactantHCID 23456997HCID 23456997—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 59304065HCID 5930406568%

Reaction Steps

To a solution of 3-hydroxy-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-1-butanone (4.00 g, 92% pure, 17.5 mmol), 3-N,N-dimethylaminobenzoic acid (3.13 g, 19.0 mmol), and DMAP (1.85 g, 15.2 mmol) in CH2Cl2 (50 ml) was added N,N′-dicyclohexylcarbodiimine (DCC) (4.31 g, 20.9 mmol) in CH2Cl2 (15 ml). The reaction medium was stirred at room temperature for 70 h. Then, the mixture was acidified with concentrated HCl and extracted twice with ether and washed with water, saturated aqueous NaHCO3 and then with saturated aqueous NaCl. Finally, the organic phases were dried over Na2SO4, concentrated at 50-60°/0.03 mbar) and purified by flash-chromatography over SiO2 (cyclohexane/AcOEt=97:3). 4.20 g of product were thus obtained (yield: 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723286B2
Source datasetuspto-grants-2010_05
ORD IDord-a77e69f673fe4635875b5f09b2964015
Source noteuspto-grants-2010_05