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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478982Generated: October 30, 2026

HCID 86585165, compound → HCID 86585164, compound

https://huagongshe.com/reaction/478982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86585165HCID 86585165—
ReactantHCID 178418361HCID 178418361—
ProductHCID 86585164HCID 86585164100.1%

Reaction Steps

39.6g (0.2 mol) of3,5-dinitrobenzyl alcohol, 23.7 g (0.3 mol) of pyridine and 200 ml of methyl ethyl ketone were introduced into a reactor and dissolved by stirring under a nitrogen gas stream at about 70° C. 35.3 g (0.2 mol) of pelargonic acid chloride was dissolved in 100 ml of methyl ethyl ketone and the resultant solution was added dropwise into the reactor as described above. After the completion of the addition, the mixture was refluxed and stirred under nitrogen for about 2 hours. Then the reactor was cooled by allowing to stand and pyridine hydrochloride was removed by filtration. The filtrate was concentrated and purified by using a column to give 50.8 g of 3,5-dinitrobenzyl pelargonate. 33.8 g of 3,5-dinitrobenzyl pelargonate and 4 g of a catalyst (5% palladium carried on active carbon) were introduced into a hydrogenation apparatus and reduced with hydrogen. After filtration and concentration, 27.8 g (0.1 mol) of 3,5-diaminobenzyl pelargonate was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642393B2
Source datasetuspto-grants-2003_11
ORD IDord-265d4ea3242649bd921024f8a51e6d0f
Source noteuspto-grants-2003_11