HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → Beta-naphthyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | alpha-Bromoisopropyl 2-naphthyl ketone | HCID 12587407 | — |
| Solvent | Water | HCID 962 | — |
| Product | Beta-naphthyl ketone | HCID 10945915 | 146.9% |
Reaction Steps
0.75 g of sodium azide was added to a mixture comprising 1.59 g of α-bromoisopropyl 2-naphthyl ketone and 40 ml of dimethyl sulfoxide, and the mixture was reacted at 50° C. for 1.5 hours. The reaction mixture was put into water and extracted with ethyl acetate, followed by washing with water. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: ethyl acetate/n-hexane=1/9) to obtain 1.19 g of oily α-azideisopropyl 2-naphthyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039420B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-920a9465e4d6450b90bffdad950ec108 |
| Source note | uspto-grants-2011_10 |