HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(Bromomethyl)-1-methoxy-2-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 1-Methoxy-4-methyl-2-nitrobenzene | HCID 67058 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(Bromomethyl)-1-methoxy-2-nitrobenzene | HCID 11579648 | 70% |
Reaction Steps
A solution of 4-methyl-2-nitroanisole (25 mmol), N-bromosuccinimide (25 mmol) and benzoyl peroxide (2.5 mmol) in carbon tetrachloride (100 mL) was heated at reflux for 18 h. The heated mixture was then poured into water. A solid precipitate formed and was separated by filtration. The aqueous filtrate was extracted with carbon tetrachloride (3×50 mL). The extract was concentrated under reduced pressure to yield a solid product. The solid products (the filtered precipitate and product of evaporating the extract) were combined and recrystallized from ethyl acetate-hexane to yield 4-methoxy-3-nitro benzyl bromide as a crystalline product in 70-75% yield. m.p. 110-112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106033B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-2366d8e276074115ab25da0842cd367e |
| Source note | uspto-grants-2012_01 |