HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Chloro-5-hydroxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 3-Chloro-5-methoxybenzaldehyde | HCID 21904633 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Chloro-5-hydroxybenzaldehyde | HCID 21904648 | 25% |
Reaction Steps
A solution of 3-chloro-5-methoxybenzaldehyde (22.8 g, 134 mmol; see step (i) above) in CH2Cl2 (250 mL) was cooled to 0° C. Boron tribromide (15.8 mL, 167 mmol) was added dropwise over 15 min. After stirring, the reaction mixture for 2 h, H2O (50 mL) was added slowly. The solution was then extracted with Et2O (2×100 mL). The organic layers were combined, dried (Na2SO4), filtered and concentrated in vacuo. Flash chromatography on silica gel eluting with Hex:EtOAc (4:1) afforded the sub-title compound (5.2 g, 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700582B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-9a8d9a7e134348f6ba779e41e8767be9 |
| Source note | uspto-grants-2010_04 |