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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186962Generated: November 2, 2026

tert-Butyl piperazine-1-carboxylate → tert-Butyl-4-[2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)propyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/1186962

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-(4-Methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)propanalHCID 59568726—
SolventDichloromethaneHCID 6344—
Producttert-Butyl-4-[2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)propyl]piperazine-1-carboxylateHCID 66643993—

Reaction Steps

In a 100 mL round bottom flask, 2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)propanal (100 mg, 0.49 mmol, 1.0 eq) and Boc-piperazine (91 mg, 0.49 mmol, 1.0 eq) was dissolved in DCM (10 mL). To above solution was added sodium triacetoxyborohydride (208 mg, 0.98 mmol, 2.0 eq). The reaction was stirred at r.t. for 16 hr. The reaction was then diluted with DCM (10 mL), washed with aqueous bicarbonate, water and brine. The organic phase was dried over MgSO4, filtered and concentrated. The product was obtained after purification by flash column chromatography (5% MeOH/DCM). LC-MS (IE, m/z): 375.41 [M+1]+; tR=2.47 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673920B2
Source datasetuspto-grants-2014_03
ORD IDord-e7acfbceccc54487976ceae135a0b3a4
Source noteuspto-grants-2014_03