HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 68706126, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl [(4-phenylpiperidin-4-yl)methyl]carbamate | HCID 49760176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68706126 | HCID 68706126 | — |
Reaction Steps
To a solution of (4-phenylpiperidin-4-ylmethyl) carbamic acid tert-butyl ester (2.1 mmol) in CH2Cl2 is added acetic anhydride (3.1 mmol) and triethylamine (3.1 mmol) at 0° C. The reaction mixture is stirred at room temperature for 2.5 h then the bulk of solvent is concentrated in vacuo. After the residue is suspended in AcOEt, the mixture is washed with water and brine, dried over MgSO4, filtered, and concentrated in vacuo to give (1-acetyl-4-phenylpiperidin-4-ylmethyl)carbamic acid tert-butyl ester, which is directly used for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07704996B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-026b8dbfbef745ff9c3e7b97d39f684b |
| Source note | uspto-grants-2010_04 |