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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692344Generated: November 1, 2026

Hydrazine hydrate (1:1) → Tert-butyl 3-hydrazinylazetidine-1-carboxylate

https://huagongshe.com/reaction/1692344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantTert-butyl 3-iodoazetidine-1-carboxylateHCID 11000522—
SolventEthanolHCID 702—
ProductTert-butyl 3-hydrazinylazetidine-1-carboxylateHCID 5804229194.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

Tert-butyl 3-iodoazetidine-1-carboxylate (142 g, 0.5016 mol) and hydrazine hydrate (245.21 mL, 5.02 mol) were mixed in ethanol (284 mL) and the reaction was heated to 85° C. for 48 hours under nitrogen. The reaction was cooled and the ethanol was removed in vacuo. The residue was partitioned between water (200 mL) and dichloromethane (300 mL), the water layer was re-extracted with dichloromethane (2×200 mL), the combined organics were dried over anhydrous magnesium sulphate, filtered and concentrated in vacuo to give the title compound as a colourless oil, (88.37 g). This compound was used immediately in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153814B2
Source datasetuspto-grants-2012_04
ORD IDord-c6cd9bfb7a654a1a9e06426dd89970ab
Source noteuspto-grants-2012_04