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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36965Generated: October 28, 2026

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

https://huagongshe.com/reaction/36965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium bisulfateHCID 516920—
Reactant1-[2-(4-Fluorophenyl)-4,4-dimethylcyclopenten-1-yl]-4-(methylthio)benzeneHCID 10448244—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanol--water (1/1)HCID 22242641—
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. K2SO4 ]in 2 mL of water. After stirring for 4 hours, 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-dimethyl cyclopenten-1-yl]-4-(methylsulfonyl)benzene (41 in Synthetic Scheme X when R1 and R2 =CH3, RS=F, R10 =SO2CH3, and R3, R4, R6, R7, R8, R9, R11 and R12=H) as a colorless solid: NMR (CDCl3) δ1.24 (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 numberUS05418254
Source datasetuspto-grants-1995_05
ORD IDord-c7daf79554c0457da16dde866a4e6ef1
Source noteuspto-grants-1995_05