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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742467Generated: October 28, 2026

Hydrazine → 1,2,2,6,6-Pentamethyl-4-piperidinyl Carbazate

https://huagongshe.com/reaction/1742467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantPhenyl 1,2,2,6,6-Pentamethyl-4-piperidinyl CarbonateHCID 20085740—
SolventMethanolHCID 887—
Product1,2,2,6,6-Pentamethyl-4-piperidinyl CarbazateHCID 53864806—

Reaction Steps

Into a 250 ml 3-neck flask was added 20.0 grams (0.069 mole) of phenyl 1,2,2,6,6-pentamethyl-4-piperidinyl carbonate and 100 mls of methanol. The flask was equipped with a magnetic stirrer, thermometer, reflux condenser and dropping funnel containing 3.8 grams (0.076 mole) of 64% aqueous hydrazine. The hydrazine was added slowly to the stirring methanol solution at room temperature. There was a slight exotherm. The reaction mixture was stirred for 5 hours at room temperature at which point liquid chromatography indicated the reaction was complete. The methanol was stripped off on a rotating evaporator under reduced pressure and the residue was dissolved in 150 ml MtBE. The MtBE solution was washed 3 times with 25 ml portions of 5% NaOH saturated with sodium chloride to remove the phenol that was generated. The MtBE layer was dried over anhydrous MgSO4, filtered and the MtBE stripped off on a rotating evaporator under reduced pressure. The residue was a white solid (m.p. 90°-94° C.) weighing 14.3 grams (90.5% crude yield). Liquid chromatography indicated the product was one component. The infrared spectrum contained a strong carbonyl peak at 1710 cm-1 and a moderate peak at 1625 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338853
Source datasetuspto-grants-1994_08
ORD IDord-283e5a5e9bff4afeae833f80bf3c607c
Source noteuspto-grants-1994_08