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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534677Generated: November 3, 2026

m-Chloroperbenzoic acid → HCID 67865713, compound

https://huagongshe.com/reaction/1534677

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 67917128HCID 67917128—
SolventDichloromethaneHCID 6344—
ProductHCID 67865713HCID 67865713—

Reaction Steps

(2S)-2,3-Dimethylbutyl-p-tolylsulfoxide (10) (52 mg, 0.2 mmol) was dissolved in 1.0 mL of anhydrous dichloromethane and 60 mg (0.3 mmol) of 3-chloroperoxybenzoic acid (80-85%, Sigma) added with stirring. The reaction mixture was stirred for 2 h and quenched with 10% sodium bicarbonate. More dichloromethane was added and the combined organic extracts were washed with aqueous sodium sulfite and brine and dried with MgSO4. The solvent was removed in vacuo and the crude sulfone was purified by silica gel flash chromatography using hexane ethyl acetate mixtures to afford sulfone (12) as a colorless oil. For analytical purposes this was also purified by HPLC (Zorbax Sil 9.4×25 cm column) using 10% ethyl acetate in hexane to give 42 mg of pure (2S)-sulfone (12): [α]D20 =+17 (c=3.5 in CHCl3); MS m/z (relative intensity) 240 (M+, 3), 197 (5), 157 (100), 92 (19), 91 (27), 85 (25), 84 (31), 43 (72); 1H NMR δ0.77 (3H, d, J=7 Hz), 0.82 (3H, d, J=7.0 Hz), 1.00 (3H, d, J=7.0 Hz), 1.66-1.98 (2H, m), 2.45 (3H, s, CH3 -Aryl), 2.86 (1H, dd, J=8, 11 Hz), 3.06 (1H, dd, j=4, 12 Hz), 7.35 (2H, d, J=7.0 Hz, H-aryl ortho), 7.75 (2H, d, J=8, H-aryl ortho). Anal. Calcd. for C13H20O2S: C, 64.96; H, 8.39; S, 13.34. Found C13H20O2S: C, 65.05; H, 8.37; S, 13.24

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089647
Source datasetuspto-grants-1992_02
ORD IDord-5d5fd90e391d440c94a96399e5311ca2
Source noteuspto-grants-1992_02