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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198140Generated: November 1, 2026

Methanol → 1-Aminocarbonyl-4-nitroxypiperidine

https://huagongshe.com/reaction/1198140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantPotassium cyanateHCID 11378442—
ReactantHCID 15068866HCID 15068866—
SolventAcetic AcidHCID 176—
Product1-Aminocarbonyl-4-nitroxypiperidineHCID 15068855—

Reaction Steps

7.1 g. 4-Nitroxypiperidine are dissolved in 60 ml. water and 30 ml. methanol and mixed with 16.2 g. potassium cyanate. After the dropwise addition of 12 ml. glacial acetic acid, stirring is continued at ambient temperature for 4 hours. The inorganic salts are precipitated out by the addition of 100 ml. ethyl acetate. After suction filtration, the aqueous phase is separated off and the organic phase is dried with anhydrous sodium sulphate. After suction filtration, the filtrate is evaporated in a vacuum. The residue is triturated with diethyl ether and the crystals are filtered off with suction. There are obtained 8.3 g. of the title compound, i.e. 89% of theory; m.p. 110°-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05280031
Source datasetuspto-grants-1994_01
ORD IDord-3f33edc990c240d8a7c498c6651f32ff
Source noteuspto-grants-1994_01