HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Hydroxy-4,5-dimethoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,4,5-Trimethoxybenzaldehyde | HCID 20525 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Hydroxy-4,5-dimethoxybenzaldehyde | HCID 10986908 | 102.1% |
Reaction Steps
A solution of boron trichloride (50 mL, 1.0 M solution in CH2Cl2) was slowly added to a solution of 2,4,5-trimethoxybenzaldehyde (3.92 g, 20 mmol) in CH2Cl2 (200 mL) at −78° C. (dry ice/acetone bath). The mixture was warmed to room temperature and stirred for three hours. 10 mL of HCl (37%) aqueous solution was poured into the resulting solution at 0° C. and extracted with CH2Cl2 (150 mL×3). The combined organic layer was washed with saturated aqueous NaCl (200 mL×2), water (100 mL×1), dried over MgSO4, and evaporated to afford 3.72 g of a light brown solid (3.72 g, 99%): 1H-NMR (400 MHz, CDCl3) δ3.88 (s, 3H), 3.94 (s, 3H), 6.47 (s, 1H), 6.91 (s, 1H), 9.70 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105680B1 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-10ce18f2773d4d82adfed736c16875f5 |
| Source note | uspto-grants-2006_09 |