HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → (2-Chloro-5-methoxy-4 nitrobenzyl)-phosphonic acid diethylester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | 1-Chloro-4-methoxy-2-methyl-5-nitrobenzene | HCID 15864566 | — |
| Reactant | 1-(Bromomethyl)-2-chloro-5-methoxy-4-nitrobenzene | HCID 67813968 | — |
| Reactant | 1-Chloro-2-dibromomethyl-4-methoxy-5-nitro-benzene | HCID 67814560 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2-Chloro-5-methoxy-4 nitrobenzyl)-phosphonic acid diethylester | HCID 86697809 | — |
Reaction Steps
A mixture of 1-Bromomethyl-2-chloro-5-methoxy-4-nitro-benzene, 1-Chloro-4-methoxy-2-methyl-5-nitro-benzene and 1-chloro-2-dibromomethyl-4-methoxy-5-nitro-benzene (Compound 56G, 24 g, 1:015:0.5) in toluene (100 mL) were treated with triethylphosphite (15.6 g, 94.2 mmol) and heated to reflux for 24 hrs. Toluene and triethylphosphite were distilled off under reduced pressure. The residue was treated with hot diisopropyl ether to give 10 g of the required compound as dark yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133224B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-99404d6ffef2434da3fcdc67602480b5 |
| Source note | uspto-grants-2015_09 |