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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505684Generated: November 2, 2026

tert-Butyl carbazate → HCID 89924517, compound

https://huagongshe.com/reaction/1505684

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl carbazateHCID 70091—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Azaspiro(4.5)-decane-2,8-dioneHCID 11412594—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 89924517HCID 89924517150.8%

Reaction Steps

A solution of 1-Aza-spiro[4.5]decane-2,8-dione (Chembridge corporation, 800 mg; 4.78 mmol; 1.0 eq.) and hydrazinecarboxylic acid tert-butyl ester (309 mg; 2.34 mmol; 1.1 eq.) in AcOH (5 mL) was stirred at RT for 5 min. Sodium cyanoborohydride (133 mg; 2.13 mmol; 1.0 eq.) was then added and the reaction mixture was stirred O/N at RT. It was then diluted with water and basified to pH 9 by addition of a 5N solution of NaOH. During the addition, the reaction mixture was maintained at 20° C. by addition of crushed ice. It was extracted with DCM and the combined organic phases were washed with brine, dried over magnesium sulfate, filtered and concentrated to give the title compound as a yellow oil (1.0 g, 98%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216991B2
Source datasetuspto-grants-2015_12
ORD IDord-74c7574ca62c4a9e94e272dcfecc8b4f
Source noteuspto-grants-2015_12