HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624032Generated: October 31, 2026
Antimony trichloride → HCID 71114847, compound
https://huagongshe.com/reaction/1624032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Antimony trichloride | HCID 24814 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (4-Chloro-2-fluorophenyl)boronic acid | HCID 4193595 | — |
| Reactant | 2-Cyclopenten-1-one, 5,5-dimethyl- | HCID 11073371 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 71114847 | HCID 71114847 | 87.2% |
Reaction Steps
A solution of 5,5-dimethylcyclopent-2-en-1-one (42.0 g, 343.15 mmol), 4-chloro-2-fluorophenylboronic acid (94.47 g, 514.72 mmol), sodium acetate (56.30 g, 686.30 mmol), acetic acid (1130 mL), Pd(OAc)2 (7.70 g, 34.31 mmol), and antimony trichloride (7.83 g, 34.31 mmol) are stirred at ambient temperature for 16 hours. The solvent is evaporated to low volume and the residual acetic acid is removed using toluene. MTBE (500 mL) is added and the resulting precipitate is filtered off and discarded. The MTBE solution is washed with water (500 mL), aq. NaHCO3 (2×300 mL), dried over MgSO4, filtered, and concentrated to dryness. The residue is purified by silica gel flash chromatography, eluting with hexane to hexane 10% MTBE to give the title compound (72 g, 87%). 1H NMR (300.16 MHz, CDCl3) δ 7.21-7.06 (m, 3H), 3.67-3.59 (m, 1H), 2.81-2.72 (m, 1H), 2.41-2.31 (m, 1H), 2.21 (ddd, J=12.6, 6.3, 2.2 Hz, 1H), 1.89 (t, J=12.3 Hz, 1H), 1.159 (s, 3H), 1.137 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778984B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-93208d0732a8490da23122490ecddb6c |
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| Source note | uspto-grants-2014_07 |
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