HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzosuberone → HCID 15751789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzosuberone | HCID 70003 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15751789 | HCID 15751789 | 93.3% |
Reaction Steps
Following the procedure of Example 1, step 1, 26.02 g (0.162 mol) of 1-benzosuberone in 250 ml of anhydrous ether was reacted with 68.0 ml (0.204 mol) of 3.0M methyl magnesium bromide in ether to afford 26.65 g (93%) of the title product as a yellow oil. NMR δ(CDCl3) 1.59 (3H, s), 1.77-1.97 (6H, m), 2.83-2.96 (2H, m), 7.06-7.24 (3H, m), 7.67 (1H, d of d, J=7.6 and 1.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254561 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-e4f54d521f29411997464bb8e7258346 |
| Source note | uspto-grants-1993_10 |