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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406342Generated: October 29, 2026

tert-Butyl carbazate → HCID 66777612, compound

https://huagongshe.com/reaction/406342

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl carbazateHCID 70091—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantEthyl 5-oxo-5-[3-(trifluoromethyl)phenyl]pentanoateHCID 24727515—
SolventAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66777612HCID 66777612—

Reaction Steps

Ethyl 5-oxo-5-(3-trifluoromethylphenyl)pentanoate (CAS No. 898777-75-8, 330 mg) and tert-butyl carbazate (227 mg) were dissolved in a mixed solvent of THF (6 mL) and acetic acid (3 mL). After stirring at room temperature for 25 minutes, sodium cyanoborohydride (108 mg) was added. After further one hour and 30 minutes, sodium cyanoborohydride (108 mg) was added and the mixture was stirred at room temperature for one hour. A saturated sodium bicarbonate solution and diethyl ether were added to the reaction solution, and the organic layer was separated. The resulting organic layer was washed with a saturated sodium bicarbonate solution and then dried over anhydrous sodium sulfate. The drying agent was separated by filtration and then the organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound (324 mg). The property values of the compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754100B2
Source datasetuspto-grants-2014_06
ORD IDord-d69413fe023f46948615c7f96f1bddd4
Source noteuspto-grants-2014_06