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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727248Generated: November 1, 2026

Triethylamine → 2-diazocyclohexane-1,3-dione

https://huagongshe.com/reaction/1727248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,3-CyclohexanedioneHCID 10434—
Reactant4-Acetamidobenzenesulfonyl azideHCID 5129185—
SolventDichloromethaneHCID 6344—
Product2-diazocyclohexane-1,3-dioneHCID 11062449—

Reaction Steps

A mixture of 4-acetamidobenzenesulphonylazide (25 g, 104 mmol) and triethylamine (36 ml, 250 mmol) in dichloromethane maintained at a temperature below 30° C. by external cooling is treated dropwise by a solution of cyclohexane-1,3-dione (13 g, 115 mmol) in 200 ml of dichloromethane. The reaction mixture is stirred for 75 minutes at ambient temperature then filtered on Celite. After concentration to approximately 300 ml, the filtrate is washed with water then dried over sodium sulphate. The brown-yellow solid (14 g; 88%) obtained by evaporation of the solvent under reduced pressure is similar to that obtained in Example 55.1, and is used as it is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495021B2
Source datasetuspto-grants-2009_02
ORD IDord-48956b759ef4424a801790be8f20d1fb
Source noteuspto-grants-2009_02