HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408084Generated: October 31, 2026
Sodium Iodide → tert-Butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1408084
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 | US08916569B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-8e61929c6fe24f4f8b15c2ae52ae2cde |
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| Source note | uspto-grants-2014_12 |
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