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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37536Generated: October 28, 2026

Potassium bisulfate → 1-[2-(4-Fluorophenyl)-4,4-dimethyl-1-cyclopentenyl]-4-methylsulfonylbenzene

https://huagongshe.com/reaction/37536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
Reactant1-[2-(4-Fluorophenyl)-4,4-dimethylcyclopenten-1-yl]-4-(methylthio)benzeneHCID 10448244—
ReactantMethanol--water (1/1)HCID 22242641—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
Product1-[2-(4-Fluorophenyl)-4,4-dimethyl-1-cyclopentenyl]-4-methylsulfonylbenzeneHCID 984107938%

Reaction Steps

A solution of 120 mg (0.39 mmol) of 1-[2-(4-fluorophenyl)-4,4-dimethylcyclopenten-1-yl]-4-(methylthio)benzene (Step 9) in 3 mL of methanol/water (1:1) was slowly treated with 470 mg (0.76 mmol) of Oxone® [2 KHSO5.KHSO4 ] in 2 mL of water. After stirring for 4 h, the solvent was removed in vacuo. The residue was dissolved in ethyl acetate and washed with water and brine, dried (MgSO4), and reconcentrated. Purification by silica gel chromatography (MPLC) with hexane/ethyl acetate (5:1) and subsequent lyophilization from acetonitrile/water (1:1) gave 50 mg (38%) of 1-[2-(4-fluorophenyl)-4,4-dimethylcyclopenten-1-yl ]-4-(methylsulfonyl)benzene (41 in Synthetic Scheme X when R1 and R2 =CH3, R5 =F, R10 =SO2CH3, R3, R4, R6, R7, R8, R9, R 11, and R12 =H) as a colorless solid: NMR (CDCl3) d 1.24 (s, 6H), 2.71 (s, 4H), 3.4 (s, 3H), 6.92 (t, J=8 Hz, 2H), 7.05-7.12 (m, 2H), 7.30 (d, J=9 Hz, 2H), 7.75 (d, J=9 Hz, 3H); MS (EI) m/e (rel intensity) 344 (100), 329 (33), 250 (18), 235 (20), 109 (35), 69 (44); HRMS. Calc'd for C20H21FO2S: 344.1246. Found: 344.1272.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420287
Source datasetuspto-grants-1995_05
ORD IDord-0a6f0361262e4fd889323b1c26c6a860
Source noteuspto-grants-1995_05