HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Nitrooxy-piperidine-1-carboxylic acid 4-nitro-phenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | Piperidin-4-yl nitrate hydrochloride | HCID 66753481 | — |
| Solvent | Acetonitrile tetrahydrofuran | HCID 22177404 | — |
| Product | 4-Nitrooxy-piperidine-1-carboxylic acid 4-nitro-phenyl ester | HCID 59178208 | — |
Reaction Steps
To a solution of Piperidin-4-yl nitrate hydrochloride (INTERMEDIATE 13, Step B) (0.40 g, 2.20 mmol) and Et3N (0.67 g, 6.60 mmol) in THF/CH3CN 2/1 (24 mL) was added 4-Nitrophenyl chloroformate (0.44 g, 2.20 mmol) as solid. After stirring at rt over night, the mixture was concentrated. The residue was diluted with EtOAc and washed with NaH2PO4 5%. The organic layer was dried over MgSO4 and concentrated. The residue was purified by flash chromatography (Biotage SP1; column SNAP 50; TLC method: n-hexane/ethyl acetate 7/3; Rf=0.37), affording the title product as a white solid. 1H-NMR (300 MHz, CDCl3); δ 8.36-8.25 (2H, m), 7.39-7.28 (2H, m), 5.30-5.18 (1H, m), 4.00-3.50 (4H, m), 2.20-2.06 (2H, m), 2.02-1.86 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119806B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-ecdbe1098567436b989849284fbc01fd |
| Source note | uspto-grants-2012_02 |