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
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), 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09301951B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-7ff6d5d18bca41959104922161d7c242 |
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| Source note | uspto-grants-2016_04 |
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