HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-Bromo-4-(dimethylamino)biphenyl-2-carboxylic acid → (4'-Bromo-4-(dimethylamino)biphenyl-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-Bromo-4-(dimethylamino)biphenyl-2-carboxylic acid | HCID 59266564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (4'-Bromo-4-(dimethylamino)biphenyl-2-yl)methanol | HCID 59266574 | 98% |
Reaction Steps
4′-bromo-4-(dimethylamino)biphenyl-2-carboxylic acid (1.34 g, 4.19 mmol) in THF (40 mL) was cooled to 0° C. Borane tetrahydrofuran complex (8.37 mL, 8.37 mmol) was added dropwise over 15 min. and allowed to warm up to r.t. overnight. The reaction was diluted with EtOAc and washed with water, saturated ammonium chloride, and then brine. The organic layer was dried over MgSO4, filtered and evaporated to give (4′-bromo-4-(dimethylamino)biphenyl-2-yl)methanol (1.25 g, 4.08 mmol, 98% yield) as a white solid. 1H NMR (500 MHz, CHLOROFORM-d) δ ppm 2.93-3.05 (m, 6H) 4.58 (s, 2H) 6.72 (dd, J=8.55, 2.75 Hz, 1H) 6.90 (d, J=2.75 Hz, 1H) 7.14 (d, J=8.55 Hz, 1H) 7.21-7.25 (m, 2H) 7.44-7.55 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08563505B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-335509e11a5a4b3da569bd77234f2f19 |
| Source note | uspto-grants-2013_10 |