HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrobenzaldehyde → [Hydroxy-(3-nitro-phenyl)methyl]-phosphonic acid dimethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylphosphite | HCID 21884954 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | [Hydroxy-(3-nitro-phenyl)methyl]-phosphonic acid dimethyl ester | HCID 11299958 | 77% |
Reaction Steps
3-Nitrobenzaldehyde (20 g, 0.132 mol) was dissolved in 100 mL of ethyl acetate. Triethylamine (22 mL, 0.158 mol, 1.2 eq) was added, followed by dimethylphosphite (15.7 mL, 0.171 mmol, 1.3 eq) and the mixture was stirred at room temperature. After 2 hours the mixture was diluted with 150 mL of ethyl acetate and washed with saturated aqueous ammonium chloride (2×50 mL) and water (50 mL). The organic layer was dried over Na2SO4 and concentrated under reduced pressure. The residue was treated with ethyl ether to obtain a beige solid, which was filtered and dried under vacuum at 40° C. for 1 h (26.7 g, 77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541575B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-6b6d0775abb64f6ba1883c5aa00c22cb |
| Source note | uspto-grants-2013_09 |