HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Bromo-naphtho[2,3-b]furan-4,9-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Trimethylsilyl-naphtho[2,3-b]furan-4,9-dione | HCID 10849666 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Bromo-naphtho[2,3-b]furan-4,9-dione | HCID 396287 | 90.2% |
Reaction Steps
To the solution of 0.8 gram (3.0 mmoles) of 2-trimethylsilyl-naphtho[2,3-b]furan-4,9-dione in 20 mL of acetonitrile at room temperature, 0.53 grams (3.3 mmoles) of bromine in 20 mL of acetonitrile was added dropwise over 5 minutes. The mixture was further stirred for 30 minutes at room temperature, and then evaporated to dryness. The residue was crystallized in ethanol/water. Pure crystal product was filtered and dried under vacuum. 0.75 grams of product (yield 90%) was obtained and characterized by 1H NMR and mass spectrum. 1H NMR (in CDCl3) δ 6.96 (s, 1H), 7.76-7.82 (m, 2H), 8.18-8.25 (m, 2H). Mass (M+H) is 277 and 279.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150530B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-52f28cb10b2042dc9c02479b5da646e6 |
| Source note | uspto-grants-2015_10 |