HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Benzyloxy-5-hydroxybenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Benzyloxy-5-hydroxybenzonitrile | HCID 21904367 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Borane;tetrahydrofuran | HCID 2723981 | — |
| Product | 3-Benzyloxy-5-hydroxybenzylamine | HCID 21904365 | — |
Reaction Steps
3-benzyloxy-5-hydroxybenzonitrile (225 mg, 1 mmol) was dissolved in 2 mL THF 2 mL of BH3-THF (1.5 M in THF and ether) was added dropwise, then the mixture was heated at reflux temperature for 3 hours. After cooling, the mixture was carefully poured to 3M HCl (ice cooled) and allowed to stir for 20 hours at room temperature. The mixture was neutralized with solid NaHCO3, thus the product precipitated as a white solid. The product was collected by filtration, washed with water, and dried (140 mg, 61%): MP 164-166° C. (dec); 1H NMR (DMSO-d6, 400 MHz) δ 9.28 (br, 1H), 7.41 (d, 2H, J=6.9 Hz), 7.36 (dd, 2H, J=7.0 and 7.6 Hz), 7.30 (dd, 1H, J=7.0 and 6.6 Hz), 6.43 (s, 1H), 6.32 (s, 1H), 6.21 (dd, 1H, J=2.2 and 2.0 Hz), 4.99 (S, 2H), 3.57 (S, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772216B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-328efd5108e14930a4b0fb22827cf48a |
| Source note | uspto-grants-2010_08 |