HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Diethoxyethylamine → HCID 178467945, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Diethoxyethylamine | HCID 69524 | — |
| Reactant | Methyl 3-bromobenzimidate hydrochloride | HCID 14685566 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178467945 | HCID 178467945 | — |
Reaction Steps
To a solution of methyl 3-bromobenzenecarboximidoate hydrochloride (Step 1 above) in MeOH (10 mL) at 0° C. was added [2,2-bis(ethyloxy)ethyl]amine (1.74 mL; 12 mmol) in one portion and the mixture was gradually warmed to room temperature (overnight). The mixture was concentrated in vacuo, partitioned between CH2Cl2/1M NaOH and the layers were separated. The aqueous layer was extracted with CH2Cl2 (×2), combined organics were washed (H2O, brine), dried over Na2SO4, filtered and concentrated in vacuo affording the title compound as a light brown oil which was used directly for Step 3 below. LC/MS (method A) tR 1.25 min, m/z 315, 317 (M+H, Br isotopes, 4%), 223, 225 (M+H−2EtOH, Br isotopes, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633175B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-838497316b9c4e5ead04a5837b5021eb |
| Source note | uspto-grants-2014_01 |