HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-nitro-2,2-dimethyl-3-bromomethyl-2H-1-benzopyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-nitro-2,2,3-trimethyl-2H-1-benzopyran | HCID 15711881 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 6-nitro-2,2-dimethyl-3-bromomethyl-2H-1-benzopyran | HCID 19387104 | 90.5% |
Reaction Steps
A solution of 6-nitro-2,2,3-trimethyl-2H-1-benzopyran (33.0 g, 0.151 mol) and benzoyl peroxide (0.020 g) in carbon tetrachloride (330 ml) were heated to 50° C. and N-bromo succinimide (26.8 g, 0.15 mol) was added. The mixture was heated at reflux for eighteen hours and then water and aqueous ferrous sulfate were added. The organic phase was separated and evaporated under reduced pressure, and the residue washed with pentane to give 40.45 g of 6-nitro-2,2-dimethyl-3-bromomethyl-2H-1-benzopyran, m.p. 107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05447943 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-bafd0644e2214aabaf2574812f9b89d8 |
| Source note | uspto-grants-1995_09 |