Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197490Generated: October 30, 2026

Triethylamine → tert-Butyl 4-(hydroxyimino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1197490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
SolventMethanolHCID 887—
Producttert-Butyl 4-(hydroxyimino)piperidine-1-carboxylateHCID 1546292463.8%

Reaction Steps

15.5 g (77.6 mmol) of N-Boc-4-piperidone was refluxed for one hour in methanol in the presence of 7.0 g (100.8 mmol) of hydroxylamine hydrochloride and 14.1 ml (100.8 mmol) of triethylamine. Then, methanol was distilled off, and the residue was thoroughly washed with water in chloroform. The chloroform layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to give 10.6 g of N-Boc-4-hydroxyiminopiperidine as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276041
Source datasetuspto-grants-1994_01
ORD IDord-9442df58577645f18da8275ef4bf7b98
Source noteuspto-grants-1994_01