HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethyl phosphite → 6,7-Dichloro-3-dimethylphosphonomethyl-2-bromoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Reactant | 6,7-Dichloro-2-bromo-3-bromomethylquinoline | HCID 19706720 | — |
| Product | 6,7-Dichloro-3-dimethylphosphonomethyl-2-bromoquinoline | HCID 54046132 | — |
Reaction Steps
A mixture of 6,7-dichloro-2-bromo-3-bromomethylquinoline (0.74 g, 2 mmol) and trimethylphosphite (5 ml) was heated at 80°-90° C. for 2-3h. Then the excess trimethylphosphite was removed in vacuo at 70°-80° C. and the oily residue was made crystalline by treating with hexane-ethyl ether (1:1). The crystalls were collected, washed with toluene and dried in vacuo to give 0.65 g of 6,7-dichloro-3-dimethylphosphonomethyl-2-bromoquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05710139 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-a0a4ca57d2c4442987f3ccc2be08b6c1 |
| Source note | uspto-grants-1998_01 |