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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466811Generated: October 30, 2026

Ammonia → HCID 19814746, compound

https://huagongshe.com/reaction/466811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantOxalic AcidHCID 971—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 19814767HCID 19814767—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 19814746HCID 19814746—

Reaction Conditions

Temperature80 °C

Reaction Steps

A stirred solution of 1-benzyl-3-(3-chloropropyl)azetidine-3-carbonitrile (D1, 5.35 g, 0.022 mole) in methanol (75 ml) was treated cautiously with concentrated sulphuric acid (15 ml) and then heated at 80° C. for 20 h. The solution was cooled in an ice bath and a further 12 ml of concentrated sulphuric acid added. The solution was heated at 80° C. for a further 9 hours, then allowed to cool, before pouring cautiously into ice/water (400 ml) with vigorous stirring. The aqueous mixture was basified by the addition of 0.88 ammonia solution, then extracted with ethyl acetate (2 ×200 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave an orange oil, which was filtered through a basic alumina column eluting with ether. The colourless oil obtained was dissolved in ether (150 ml) and treated with a solution of oxalic acid (2.0 g, 0.022 mole) in methanol (10 ml). The title compound (D2) was filtered off as a white crystalline solid (7.25 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157160
Source datasetuspto-grants-1992_10
ORD IDord-2119b670674d4ae4bf1ab5b83f86779f
Source noteuspto-grants-1992_10