HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 3,4-Dihydroxy-5-nitrobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 5-Nitrovanillin | HCID 81134 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,4-Dihydroxy-5-nitrobenzaldehyde | HCID 5748957 | 55.4% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
35 g of 5-nitro vanillin (commercial) and 1200 ml of dichloromethane were mixed together under nitrogen and the mixture was cooled to 0° C. 533 ml of a molar solution of boron tribromide in dichloromethane were added and the mixture stood for 2 days at abmient temperature and then was concentrated. The residue was taken up cold (ice bath+methanol) in 300 ml of 2N hydrochloric acid and the mixture was stirred for two to three hours at this temperature, then left for 16 hours at ambient temperature. Extraction was carried out with ethyl acetate and the organic phase was washed, dried and concentrated to obtain 18 g of the expected product melting at >260° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728828 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-9efe6333e98c4733b21ed3413c8658d8 |
| Source note | uspto-grants-1998_03 |