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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491458Generated: October 27, 2026

Water → Tert-butyl 4-(2-(tert-butoxycarbonyl)hydrazinyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/491458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBorohydrideHCID 28123—
ReactantTert-butyl 4-[(tert-butoxycarbonyl)hydrazono]piperidine-1-carboxylateHCID 20824233—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(2-(tert-butoxycarbonyl)hydrazinyl)piperidine-1-carboxylateHCID 20824232—

Reaction Steps

150 ml of a solution of borohydride in tertahydrofurane (1.0 mol/l) is slowly added to a solution of 0.12 mole of 4-(tert-Butoxycarbonyl-hydrazono)-piperidine-1-carboxylic acid tert-butyl ester (starting compound A7) in 100 ml of dry tetrahydrofurane. After complete addition, the mixture is stirred for another 30 min after which a 100 ml of water is added to destroy the excess of borohydride. Subsequently the tetrahydrofurane is evaporated and the resulting aqeous solution extracted with diethyl ether. After drying the solvent over magnesium sulfate, the ether is evaporated. M. p.112-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531540B2
Source datasetuspto-grants-2009_05
ORD IDord-37a6c5f77283423bb64ce26cea869ed6
Source noteuspto-grants-2009_05