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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408169Generated: November 2, 2026

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

https://huagongshe.com/reaction/1408169

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), methanamine (in ethanol) (10 mL), 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. The pH value of the solution was adjusted to 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 numberUS08916569B2
Source datasetuspto-grants-2014_12
ORD IDord-9ac81cfe024f4224a41cbe62d8a6b1d2
Source noteuspto-grants-2014_12