Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585324Generated: October 31, 2026

1,3-Cyclohexanedione → HCID 22340629, compound

https://huagongshe.com/reaction/585324

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-CyclohexanedioneHCID 10434—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Amino-3,4-dimethylpyridineHCID 11007884—
ReactantHCID 22340628HCID 22340628—
SolventDichloromethaneHCID 6344—
ProductHCID 22340629HCID 22340629—

Reaction Steps

0.295 g (0.9 mmol) of 2-chloro-3-(methylcarbonylmethoxy)-4-ethylsulfonylbenzoic acid, 0.113 g (1.0 mmol) of cyclohexane-1,3-dione, 0.180 g (0.9 mmol) of N′-(3-dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride and 0.001 g of dimethyl-aminopyridine were stirred in 25 ml of CH2Cl2 at RT for 2 h. The mixture was then diluted with CH2Cl2 and washed with 0.5 N HCl, with water, with saturated NaHCO3 solution and again with water. The combined organic phases were dried over Na2SO4 and then evaporated to dryness, giving 3-oxo-1-cyclohexenyl 2-chloro-3-(methylcarbonylmethoxy)-4-ethylsulfonylbenzoate in the form of a brown resin which was sufficiently pure for the subsequent reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06930208B2
Source datasetuspto-grants-2005_08
ORD IDord-09a04ad39724402a9226e6fcd90b4c7b
Source noteuspto-grants-2005_08