HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 28431408, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 28431408 | HCID 28431408 | — |
Reaction Steps
To a solution of methyl bromoacetate (24.0 mL, 254 mmol) in anhydrous THF (264 mL) was added dropwise triethylamine (35.3 mL, 254 mmol). The cloudy mixture was treated rapidly with 4-fluorobenzylamine, and the resulting viscous mixture was stirred at ambient temperature under inert atmosphere for 18 h. THF was removed in vacuo, and the resulting residue was suspended in diethyl ether. The mixture was filtered and the solids washed with excess diethyl ether. Concentration of the filtrate in vacuo afforded the title compound as a light yellow oil. 1H NMR (400 MHz, CDCl3) δ 7.31-7.27 (m, 2H), 7.04-6.99 (m, 2H), 3.77 (s, 2H), 3.74 (s, 3H), 3.41 (s, 2H), 1.82 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820680B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-3f6eee5b695e40fa858385d260ee376a |
| Source note | uspto-grants-2010_10 |