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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225991Generated: November 2, 2026

Sodium Carbonate → 1-[2-(4-Fluorophenyl)cyclopenten-1-yl]-4-(methylthio)benzene

https://huagongshe.com/reaction/2225991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant1-(2-Bromocyclopenten-1-yl)-4-(methylthio)benzeneHCID 10265059—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product1-[2-(4-Fluorophenyl)cyclopenten-1-yl]-4-(methylthio)benzeneHCID 10613074—

Reaction Steps

Under nitrogen, 1.5 g (5.6 mmol) of 1-(2-bromocyclopenten-1-yl)-4-(methylthio)benzene (Step 2) was reacted with 1.5 g (11 mmol) of 4-fluorophenylboronic acid (Lancaster) in 30 mL of toluene, 20 mL of ethanol, and 25 mL of 2M Na2CO3 in the presence of 250 mg of Pd(PPh3)4. The reaction was vigorously stirred at reflux overnight and concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with water, dried (MgSO4), and reconcentrated. Purification by silica gel chromatography with hexane gave 1-[2-(4-fluorophenyl) cyclopenten-1-yl]-4-(methylthio)benzene (41 in Synthetic Scheme X when R5 =SCH3, R10 =F, and R1, R2, R3, R4, R6, R7, R8, R9, R11, and R12 =H) as a colorless solid. mp 46°-47° C.; NMR (CDCl3) d 2.04 (m, J=7 Hz, 2H) , 2.45 (s, 3H), 2.86, (t, J=7 Hz, 4H) , 6.86-6.94 (m, 2H) , 7 . 08 (br s, 4H) , 7.10-7.18 (m, 2H) .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344991
Source datasetuspto-grants-1994_09
ORD IDord-98b1d767a2234716a289764bc51d58d9
Source noteuspto-grants-1994_09