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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173122Generated: October 31, 2026

tert-Butyl piperazine-1-carboxylate → HCID 67517481, compound

https://huagongshe.com/reaction/2173122

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 87429801HCID 87429801—
SolventDichloromethaneHCID 6344—
ProductHCID 67517481HCID 67517481—

Reaction Steps

The crude (4-iodo-1-oxo-1,3-dihydro-2-benzofuran-5-yl)acetaldehyde (1.2 g) was dissolved in DCM (40 mL). Boc-piperazine (1.1 g, 5.9 mmol) was added into the solution, followed by addition of sodium triacetoxyborohydride (4.2 g, 20 mmol). The reaction was allowed to stir at RT overnight. The reaction was diluted with DCM, washed with sodium bicarbonate and brine, dried over MgSO4, and purified by silica gel chromatography to furnish tert-butyl-4-[2-(4-iodo-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate. LC-MS (IE, m/z): 473 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-b953d833c59f4dfa80504f9138897e7a
Source noteuspto-grants-2015_06