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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530623Generated: November 3, 2026

HCID 88932543, compound → HCID 57600137, compound

https://huagongshe.com/reaction/1530623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 88932543HCID 88932543—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 57600137HCID 5760013755%

Reaction Steps

A mixture of (E)-tert-butyl 2-(2-(tert-butyldimethylsilyloxy)ethylidene)hydrazinecarboxylate (5.1 g, 17.71 mmol) and Pd/C (0.5 g, 10%) in MeOH (100 mL) was stirred under 1 atm H2 at room temperature for 1 h. The solid was filtered off and the filtrate was concentrated. The residue was purified by silica gel chromatography eluting with EtOAc/petroleum ether (5:1) to give tert-butyl 2-(2-(tert-butyldimethylsilyloxy)ethyl)hydrazinecarboxylate (2.8 g, 55% yield) as colorless oil. LCMS (ESI) m/z: 235.3 [M-56+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-e5c4cd9b5f0141b9b765b59fc802e567
Source noteuspto-grants-2015_07