HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Ethyl 3,4,4-trimethoxypiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3,4,4-Trimethoxypiperidine | HCID 19883516 | — |
| Product | Ethyl 3,4,4-trimethoxypiperidine-1-carboxylate | HCID 3019431 | — |
Reaction Steps
The title compound was prepared by taking 3,4,4-trimethoxypiperidine (150 mg, 0.00086 mol) in Methylene chloride (10 mL, 0.2 mol) and adding Ethyl chloroformate (0.098 mL, 0.0010 mol) and Triethylamine (0.24 mL, 0.0017 mol). The reaction was stirred overnight and then quenched with NaHCO3. The crude was obtained by evaporating the organic layer and was taken to the next step as-is (210 mg, 99%). MS calculated for C11H21NO5: (M+H) 248; found 248.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700624B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-becbfeea679442c58c46818c266f9758 |
| Source note | uspto-grants-2010_04 |