Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20975Generated: October 25, 2026

Acetic Acid → 5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indole

https://huagongshe.com/reaction/20975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium CarbonateHCID 10340—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantIndole-5-carboxaldehydeHCID 589040—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-[4-(Tert-butoxycarbonyl)piperazin-1-ylmethyl]indoleHCID 6848993447%

Reaction Steps

5-Formylindole (500 mg, 3.44 mmol) was dissolved in acetonitrile (10 mL), and the solution was added with 1-(tert-butoxycarbonyl)piperazine (961 mg, 5.16 mmol), acetic acid (3.90 mL, 68.1 mmol) and sodium triacetoxyborohydride (3.65 g, 17.2 mmol) little by little, followed by stirring at room temperature for 2 hours. The reaction mixture was added with water and sodium carbonate to adjust the pH to 9, followed by extracting with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography (hexane/ethyl acetate=19/1, 7/3, 1/1) to obtain 5-[4-(tert-butoxycarbonyl)piperazin-1-ylmethyl]indole (505 mg, yield 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-40825bde11ad4d73a783930ebca6be83
Source noteuspto-grants-2010_06