HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → tert-Butyl ethyl(piperidin-4-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate | HCID 21981786 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl ethyl(piperidin-4-yl)carbamate | HCID 18677728 | 126.1% |
Reaction Steps
To a solution of 476 mg (1.42 mmol) of 1-benzyloxycarbonyl-4-(t-butoxycarbonylamino)piperidine from Step B and 0.24 mL (2.8 mmol) of ethyl iodide in 10 mL of DMF was added 85 mg (2.1 mmol) of 60% sodium hydride in mineral oil. The reaction was stirred for 16 h and was then poured into water and extracted three times with ether. The organic layers were each washed with a portion of water and brine, dried over sodium sulfate, combined and concentrated. The residue was purified by FC eluting with 15% ethyl acetate in hexanes to afford 409 mg of title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472410B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-7a5552f5c2af4dc2908bcaa633a0b984 |
| Source note | uspto-grants-2002_10 |