HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5-Bromo-2,2-diphenyl-1,3-benzodioxol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2-Diphenyl-1,3-benzodioxole | HCID 343959 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Bromo-2,2-diphenyl-1,3-benzodioxol | HCID 22319515 | — |
Reaction Steps
18.75 g of N-bromosuccinimide are added to a solution of 27.4 g of 2,2-diphenyl-1,3-benzodioxol in 80 ml of chloroform and the mixture was boiled at reflux for 20 hours. The reaction mixture was cooled and the separated succinimide was filtered off. The filtrate was washed with water, dried over sodium sulphate and the solvent was removed in a vacuum. By crystallization of the residue from ethanol, there was obtained 5-bromo-2,2-diphenyl-1,3-benzodioxol as white crystals of melting point 88°-89° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05073550 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-1f40e0ed99974a8d8d8867f12beacd33 |
| Source note | uspto-grants-1991_12 |