HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Bromo-4,5,6-trimethoxyphthalide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4,5,6-trimethoxy-2-benzofuran-1(3H)-one | HCID 230869 | — |
| Reactant | Azobisbutyronitrile | HCID 14151322 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Bromo-4,5,6-trimethoxyphthalide | HCID 21423039 | — |
Reaction Steps
4,5,6-Trimethoxyphthalide (11.4 gms; 0.05 mole), N-bromosuccinimide (8.9 gms; 0.05 mole) and azobisbutyronitrile (0.1 gms) were refluxed gently in dry carbon tetrachloride (200 mls) for 2 hours. The solution was cooled, the succinimide filtered off and the solvent removed in vacuo, leaving a yellowish solid which fumed in the air.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03963704 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-a0d3b55add8d48449dbb2f74e5aa022f |
| Source note | uspto-grants-1976_06 |