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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624032Generated: October 31, 2026

Antimony trichloride → HCID 71114847, compound

https://huagongshe.com/reaction/1624032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAntimony trichlorideHCID 24814—
ReactantSodium AcetateHCID 517045—
Reactant(4-Chloro-2-fluorophenyl)boronic acidHCID 4193595—
Reactant2-Cyclopenten-1-one, 5,5-dimethyl-HCID 11073371—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetic AcidHCID 176—
ProductHCID 71114847HCID 7111484787.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778984B2
Source datasetuspto-grants-2014_07
ORD IDord-93208d0732a8490da23122490ecddb6c
Source noteuspto-grants-2014_07