HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-(Bromomethyl)-2-fluoro-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Fluoro-4-nitrotoluene | HCID 74025 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | Sodium Bromate | HCID 23668195 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(Bromomethyl)-2-fluoro-4-nitrobenzene | HCID 21886132 | — |
Reaction Steps
To a solution of 2-Fluoro-1-methyl-4-nitro-benzene (1 g, 6.45 mmol) and sodium bromate (2.92 g, 19.33 mmol) in an EtOAc:water (12 mL:9 mL) mixture, is added dropwise via addition funnel a 3.85M solution of sodium bisulfite 5.20 mL, 19.33 mmol). The mixture is vigorously stirred for six days and then sodium bisulfite (10 mL) is added and organic layer separated and washed with aqueous saturated solution of sodium bicarbonate. The organic phase is dried with magnesium sulfate, filtered and evaporated at reduced pressure to afford a mixture of title compound and starting 2-fluoro-1-methyl-4-nitro-benzene in a 5:1 ratio (1H-NMR) which is used in the next step without further purification. ES+(m/z) 235 [M+H]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07767674B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-b41892aa70564ec396ad3593d85134ab |
| Source note | uspto-grants-2010_08 |