HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 10523080, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Chloro-o-anisic acid | HCID 76970 | — |
| Reactant | p-Bromophenethylamine | HCID 533915 | — |
| Reactant | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10523080 | HCID 10523080 | 96.5% |
Reaction Steps
A solution of 8.3 g (44.4 mmol) of 5-chloro-2-methoxybenzoic acid and 7.8 g (48.1 mmol) of carbonylbisimidazole in 200 ml of absolute THF was stirred at room temperature for 2 h. 7.7 ml (50.0 mmol) of 2-(4-bromophenyl)ethylamine and 10 ml of triethylamine were added and the resulting solution was stirred at room temperature for 24 h. The reaction solution was then poured onto water, and the deposited precipitate was filtered off with suction and washed with water. Drying of the precipitate yielded 15.8 g of the title compound in the form of a slightly yellow-colored solid. M.p.: 104-109° C. Rf (silica gel, EA/heptane 2:1)=0.66. MS (ESI): m/z=368/370 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06410573B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-5e192959dcd94b73a7c1997bc16a5231 |
| Source note | uspto-grants-2002_06 |