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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | tert-Butyl 4-(2-chloroethyl)piperazinecarboxylate | HCID 22106269 | — |
| Product | tert-Butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate | HCID 23081391 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916569B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-9ac81cfe024f4224a41cbe62d8a6b1d2 |
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| Source note | uspto-grants-2014_12 |
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