HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (3S,4R)-1-tert-butyl 3-ethyl 4-(allyloxycarbonyl)piperidine-1,3-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | 1-tert-butyl 3-ethyl (3S,4R)-4-aminopiperidine-1,3-dicarboxylate | HCID 58745494 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3S,4R)-1-tert-butyl 3-ethyl 4-(allyloxycarbonyl)piperidine-1,3-dicarboxylate | HCID 66952501 | 60.4% |
Reaction Steps
A solution of 259A (900 mg, 3.3 mmol) in CH2Cl2 (20 mL) was treated with triethylamine (0.64 mL, 4.62 mmol) and allylchloroformate (0.35 mL, 3.96 mmol) at room temperature. The mixture was stirred for four hours, then washed with 0.1 N HCl (2×10 mL), 1N NaOH (2×10 mL) and brine (10 mL). The organic layer was dried (Na2SO4), filtered and concentrated in vacuo to give 680 mg (yield: 58%) of Compound 259B as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07297695B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-13e6bc8bec2d4724a81233d2b6593fd0 |
| Source note | uspto-grants-2007_11 |