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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173294Generated: October 29, 2026

tert-Butyl piperazine-1-carboxylate → HCID 86693013, compound

https://huagongshe.com/reaction/2173294

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 77230761HCID 77230761—
SolventEthyl AcetateHCID 8857—
ProductHCID 86693013HCID 86693013—

Reaction Steps

To a flask charged with Boc-piperazine (130 mg, 0.70 mmol) and 7-bromo-1-benzofuran-3-carbaldehyde (141 mg, 0.63 mmol) was added NaBH(OAc)3 (761 mg, 2.80 mmol). The mixture was stirred at room temperture for 12 hours. Then the reaction was diluted with EtOAc (50 mL), washed with brine (15 mL), dried over Na2SO4 and concentrated. The residue was purified with prep-TLC to obtain the pure product tert-butyl 4-[(7-bromo-1-benzofuran-3-yl)methyl]piperazine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-db6006bbb3b441c59a56eacc0ef75b11
Source noteuspto-grants-2015_06