HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron Trichloride → 2,3-Dihydroxy-4-methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | 3-Methylveratrole | HCID 78215 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Dihydroxy-4-methylbenzaldehyde | HCID 53733663 | — |
Reaction Steps
To a solution of 1,2-dimethoxy-3-methyl-benzene (13.8 g, 76.66 mmol) cooled to −30° C. (dry ice/acetone) in dichloromethane (200 mL) was added boron trichloride (230 mL, 230 mmol) dropwise and the mixture was left to stir overnight at room temperature. The solution was cooled to 0° C. and ice/water was added carefully, and then extracted with excess of dichloromethane. The organic layer was washed with water, dried (Na2SO4) and the solvent was evaporated. Purification by silica gel column chromatography (10-20% EtOAc/hexane) gave the title compound as a crystalline solid: yield 9.2 g (80%). 1H NMR (400 MHz, CDCl3) δ (ppm): 11.11 (s, 1H), 9.82 (s, 1H), 7.05 (d, J=8.2 Hz, 1H), 6.81 (d, J=8.6 Hz, 1H), 5.67 (s, 1H), 2.33 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703742B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-b6ef99f27c3a460593dc87dfaa9c1fed |
| Source note | uspto-grants-2014_04 |