HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 58268614, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2-chloropyridin-3-yl)methanamine | HCID 10898820 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58268614 | HCID 58268614 | 47.5% |
Reaction Steps
To a solution of (2-chloro-3-pyridyl)methanamine (300 mg, 2.10 mmol) in dichloromethane (2 mL) at room temperature is added acetic acid anhydride (198.88 mL, 2.10 mmol) and triethylamine (293.26 mL, 2.10 mmol). After 1 h the reaction is quenched with saturated aqueous solution of sodium bicarbonate and extracted with dichloromethane. The organic layer was separated, dried over magnesium sulfate and the solvent evaporated in vacuo to afford 184 mg of N-[(2-chloro-3-pyridyl)methyl]acetamide. MS (m/z): 185 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232289B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-c4d0cc96a440433cb4c3b2dba67548cf |
| Source note | uspto-grants-2012_07 |