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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625341Generated: October 29, 2026

Sodium Iodide → tert-Butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/625341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMethylamineHCID 6329—
Reactanttert-Butyl 4-(2-chloroethyl)piperazinecarboxylateHCID 22106269—
Producttert-Butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylateHCID 23081391—

Reaction Conditions

Temperature70 °C

Reaction Steps

Into a 50-mL sealed tube, was placed tert-butyl 4-(2-chloroethyl)piperazine-1-carboxylate (300 mg, 1.21 mmol, 1.00 equiv), methylamine (in ethanol) (10 mL), and NaI (100 mg). The resulting solution was stirred for 12 h at 70° C. in an oil bath. The resulting mixture was concentrated under vacuum. The resulting solution was diluted with 3 mL of water and adjusted to pH 7-8 with sodium bicarbonate (5%). The resulting solution was extracted with 2×5 mL of dichloromethane and the organic layers combined. The resulting mixture was washed with 1×3 mL of water and 1×3 mL of brine. The resulting mixture was concentrated under vacuum. This resulted in 180 mg (crude) of tert-butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301951B2
Source datasetuspto-grants-2016_04
ORD IDord-7ff6d5d18bca41959104922161d7c242
Source noteuspto-grants-2016_04