HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 7-amino-9a-butyl-6-fluoro-1,2,9,9a-tetrahydro-3H-fluoren-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 5-Amino-2-butyl-6-fluoro-2-(3-oxobutyl)-1-indanone | HCID 17972707 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-amino-9a-butyl-6-fluoro-1,2,9,9a-tetrahydro-3H-fluoren-3-one | HCID 17972681 | 80% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
The diketone from step 1 (0.6 g, 2.14 mmol) was dissolved in toluene (15 mL) and treated with acetic acid (0.236 mL, 4.12 mmol) and pyrrolidine (0.344 mL, 4.12 mmol). The resulting solution was stirred and heated in an oil bath at 100° C. for 1.5 hours. After cooling to room temperature, the mixture was filtered through a pad of silica gel and the product was washed off with EtOAc. The filtrate and washings were concentrated under vacuum. The residue was purified by flash chromatography on a Biotage 40M KP-Sil column, eluting with 4:1 to 3:1 hexanes-EtOAc. The product containing fractions were evaporated under vacuum to provide 7-amino-9a-butyl-6-fluoro-1,2,9,9a-tetrahydro-3H-fluoren-3-one (0.45 g, 80%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157604B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-d126b477d1e245b790ef94cc03d4ccc6 |
| Source note | uspto-grants-2007_01 |