HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → HCID 23594251, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 2-(4-(bromomethyl)phenyl)acetate | HCID 11770640 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23594251 | HCID 23594251 | — |
Reaction Steps
To a stirring solution of 15 in tetrahydrofuran (0.4 M) at room temperature under nitrogen was added methylamine (7.5 eq) and triethylamine (12.0 eq). The reaction was stirred at room temperature overnight. The tetrahydrofuran was removed under reduced pressure and the resulting oil was diluted with H2O. The aqueous layer was acidified with 6N hydrochloric acid, extracted with ethyl acetate (3×), made basic with saturated sodium bicarbonate and extracted with dichloromethane (3×). The dichloromethane was dried over sodium sulfate, filtered and concentrated in vacuo to afford the product. (66%) 1H NMR (400 MHz, CDCl3) δ 7.31 (d, 2H), 7.25 (d, 2H), 3.77 (s, 2H), 3.69 (s, 3H), 3.62 (s, 2H), 2.45 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06992193B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-c071190051cc4e09aa2bdb0f7aa21a38 |
| Source note | uspto-grants-2006_01 |