HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 1-Bromo-4-(bromoacetyl)naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(4-Bromonaphthalen-1-yl)-2-diazoethanone | HCID 72337901 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Bromo-4-(bromoacetyl)naphthalene | HCID 59611043 | 51% |
Reaction Steps
1-(4-Bromonaphthalen-1-yl)-2-diazoethanone (13.8 g) was dissolved in ethyl acetate (200 mL), and hydrobromic acid solution (8.4 mL, 5.7 M in acetic acid) was added at 0° C. Reaction mixture was stirred 15 minutes, NaHCO3 solution (100 mL) was added, and mixture was stirred 10 minutes. Ethyl acetate solution was extracted twice with NaHCO3 solution (50 mL), once with brine (50 mL), and evaporated under vacuum. The oil was dissolved in DCM and purified by chromatography (0-20% ethyl acetate:hexane), giving 2-bromo-1-(4-bromo-naphthalen-1-yl)-ethanone (6.67 g, 51%) as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08669234B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-b9ae47ea60634e46b277697fc72758c0 |
| Source note | uspto-grants-2014_03 |