HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → HCID 178482641, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 3'-Bromo-4'-methoxy-1,1'-biphenyl-4-carbaldehyde | HCID 57681610 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178482641 | HCID 178482641 | 98% |
Reaction Steps
A mixture of 3′-bromo-4′-methoxy-1,1′-biphenyl-4-carbaldehyde (7.56g, 26.0 mmol), prepared in the previous step, methylamine (16.2 mL of an 8.03 M solution in ethanol; 130 mmol) and 20.0 g of anhydrous MgSO4 in 150 mL of methylene chloride was stirred under nitrogen at room temperature for 22 h. The reaction was filtered and the filtrate concentrated under reduced pressure to give N-[(E)-(3′-bromo-4′-methoxy-1,1′-biphenyl-4-yl)methylidene]-N-methylamine (7.77 g, 98%) as a brown solid, mp 115-117° C. Elemental Analysis for C15H14BrNO. Calc'd: C, 59.23; H; 4.64; N, 4.60. Found: C, 58.99; H, 4.38; N, 4.63
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534894B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-d9b704a77ab6412ea95a5bbdcdb5b2c4 |
| Source note | uspto-grants-2009_05 |