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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376523Generated: October 31, 2026

Potassium bisulfate → SC-57666

https://huagongshe.com/reaction/1376523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bisulfateHCID 516920—
Reactant1-[2-(4-Fluorophenyl)cyclopenten-1-yl]-4-(methylthio)benzeneHCID 10613074—
ReactantMeOH tetrahydrofuranHCID 21899815—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
ProductSC-57666HCID 44337354%

Reaction Steps

A solution of 1.5 g (5 mmol) of 1-[2-(4-fluorophenyl)cyclopenten-1-yl]-4-(methylthio)benzene (Step 3) in 46 mL of methanol/THF (1:1) was slowly treated with 5.2 g (8.4 mmol) of Oxone® [2 KHSO5.KHSO4.K2SO4 ] in 23 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. Recrystallization from ethyl acetate/hexane provided 960 mg (54%) of 1-[2-(4-fluorophenyl)cyclopenten-1-yl]-4-(methylsulfonyl)benzene (41 in Synthetic Scheme X when R5 =SO2CH3, R10 =F, and R1, R2, R3, R4, R6, R7, R8, R9, R11, and R12 =H) as a colorless solid: mp 138°-139° C.; NMR (CDCl3) δ 2.09 (m, J=7 Hz, 2H), 2.91 (t, J=7 Hz, 4H), 3.04 (s, 3H), 6.88-6.96 (m, 2H), 7.06-7.14 (m, 2H), 7.32 (d, J=8 Hz, 2H), 7.76 (d, J=8 Hz, 2H). MS (EI) m/e (rel intensity) 316 (100), 237 (41), 161 (13); HRMS. Calc'd for C18H17FO2S: 316.0933. Found: 316.0943. Anal. Calc'd for C18H17FO2S: C, 68.33; H, 5.42; F, 6.00; S, 10.13. Found: C, 68.08; H, 5.45; F, 6.42; S, 9.98.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663180
Source datasetuspto-grants-1997_09
ORD IDord-2b7598771c97405ba2962d52b81c6911
Source noteuspto-grants-1997_09