Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030940Generated: October 30, 2026

Diethyl azodicarboxylate → HCID 14989389, compound

https://huagongshe.com/reaction/1030940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactantethyl 4-mercaptobenzoateHCID 10845149—
ReactantHCID 14989224HCID 14989224—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14989389HCID 1498938913.5%

Reaction Steps

To a stirred solution of 5.6 parts of 1-(6-chloro-3-pyridazinyl)-4-piperidinepropanol, 4.2 parts of ethyl 4-mercaptobenzoate and 6 parts of triphenylposphine in 135 parts of tetrahydrofuran was added dropwise a solution of 4 parts of diethyl diazenedicarboxylate in 45 parts of tetrahydrofuran at 20° C. Upon complete addition, stirring was continued overnight at this temperature. The reaction mixture was evaporated and the residue was taken up in water. The product was ectracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.3 parts (13.5%) of ethyl 4-[[3-[1-(6-chloro-3-pyridazinyl)-4-piperidinyl]propyl]thio]benzoate; mp. 96.3° C. (comp. 164).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106973
Source datasetuspto-grants-1992_04
ORD IDord-5b037c08a35e47c08929a26547b22255
Source noteuspto-grants-1992_04