HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468081Generated: November 1, 2026
Boron trifluoride etherate → 6'-Bromo-5'-fluorospiro[cyclohexane-1,2'-indene]-1',4(3'H)-dione
https://huagongshe.com/reaction/1468081
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 2-(Trimethylsiloxy)-1,3-butadiene | HCID 554657 | — |
| Reactant | 6-Bromo-5-fluoro-2-methylene-2,3-dihydro-1H-inden-1-one | HCID 86706692 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6'-Bromo-5'-fluorospiro[cyclohexane-1,2'-indene]-1',4(3'H)-dione | HCID 86706693 | 53.5% |
Reaction Steps
To a cold (0° C.) solution of (buta-1,3-dien-2-yloxy)trimethylsilane (1.86 mL, 10.6 mmol) in DCM (80 mL) was 6-bromo-5-fluoro-2-methylene-2,3-dihydro-1H-inden-1-one (Intermediate 5, 2.32 g, 9.62 mmol) added. Boron trifluoride diethyl etherate (0.594 mL, 4.81 mmol) was added at 0° C. The reaction was stirred for 30 min., and then quenched with MeOH (1.0 mL). The reaction mixture was acidified with aq. 2 M HCl solution, and extracted with DCM. The organic phase was washed with brine, dried over sodium sulfate and concentrated. The product was purified by flash column chromatography using a stepwise gradient of heptane/EtOAc (7:1-3.5:1-1:1), to give the title compound (1.60 g, 53% yield). 1H NMR (500 MHz, CDCl3) δ ppm 1.83-1.94 (m, 2 H) 2.17-2.27 (m, 2 H) 2.38-2.51 (m, 2 H) 2.72 (dt, 2 H) 3.18 (s, 2 H) 7.25 (d, 1 H) 8.01 (d, 1 H); MS (ES+) m/z 311,313 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09000183B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-4bbb6cc9634a46e6bdb0a95a46331e47 |
|---|
| Source note | uspto-grants-2015_04 |
|---|