Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzothiazole | HCID 7222 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | Bis(2-methylphenyl)methanone | HCID 219387 | 52% |
Reaction Steps
Step 2 Under anhydrous conditions benzothiazole was dissolved in THF (0.35 M). At −78° C. added BuLi (1.1 eq). After 1 h at −78° C., added the amide from step 1 in THF, over 15 min. The reaction was allowed to warm to 25° C. After stirring at 25° C. for 1 day, workup with ethyl acetate and water and chromatography afforded pure tolyl ketone product (52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06916841B2 |
|---|
| Source dataset | uspto-grants-2005_07 |
|---|
| ORD ID | ord-8c62b6d0254948cea9ebdd8bea697e32 |
|---|
| Source note | uspto-grants-2005_07 |
|---|
