HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 86749594, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (4aR,8aS)-2-Benzoyloctahydroisoquinolin-6(2H)-one | HCID 70055598 | — |
| Reactant | HCID 178418676 | HCID 178418676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86749594 | HCID 86749594 | — |
Reaction Steps
Following the general procedure described in Example 25, a solution of p-fluorophenyl magnesium bromide in THF (1.0M, 2.61 mL, 2.61 mmol) was reacted with cis-2-benzoyl-6-oxodecahydroisoquinoline (670 mg, 2.61 mmol) in anhydrous THF at -78° C. Column chromatography (ethyl acetate) afforded the product, a solid (478 mg):mp 84°-85° C.; NMR (CDCl3, 200 MHz): 7.5-7.35 (m, 7H), 7.0 (t, 2H, J=8), 4.65-4.35 (m, 1H), 3.8-3.6 (m, 1H), 3.3-3.1 (m, 1H), 3.1-2.8 (m, 1H), 2.65-2.35 (m, 1H), 2.1-1.4 (m, 10 H); Anal. Calcd for C22H24FNO2 : C, 74.76, H, 6.84, N, 3.96, F, 5.38; Found: C, 74.59, H, 6.93, N, 3.79, F, 5.53.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05532243 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-97c12ffd221741bca350a96e958445db |
| Source note | uspto-grants-1996_07 |