HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → Acenaphthene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-Bromoacenaphthylene | HCID 615553 | — |
| Product | Acenaphthene | HCID 6734 | — |
Reaction Steps
After the reaction solution was cooled, separated potassium bromide was removed by filtration, methanol was distilled, washed 3 times with water, and the benzene solution was concentrated and dropwise added into cold acetone (0°~-10° C.), to obtain reprecipitate of 140 g of condensed bromoacenaphthylene. Elemental analysis showed that the composition of the condensate corresponded to (C12H4.4 Br2.7)m and the yield from acenaphthene was 76.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731493 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-07350e11e178470888e21a6234197726 |
| Source note | uspto-grants-1988_03 |