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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637417Generated: November 2, 2026

Dimethyl Sulfide → HCID 15460403, compound

https://huagongshe.com/reaction/1637417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 15460402HCID 15460402—
SolventDichloromethaneHCID 6344—
ProductHCID 15460403HCID 1546040366.1%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a solution of phenyl 6-deoxy-2,3,4-tri-O-pivaloyl-1-thio-β-L-galactopyranoside 4 (2.47 g, 5.22 mmol) in 65 mL of CH2Cl2 at -78° C. is added mCPBA (1.53 g, 8.84 mmol). The reaction mixture is allowed to warm to -15° C. and then quenched with methyl sulfide (5.3 mL, 4.48 g, 17.4 mmol) and allowed to warm to room temperature. The reaction mixture is then diluted with 50 mL CH2Cl2, extracted with H2O (100 mL), saturated NaHCO3 (100 mL), saturated NaCl (100 mL), dried over Na2SO4, filtered and concentrated to afford a white solid. The sulfoxide is purified using flash chromatography (15% EtOAc/petroleum ether) to afford 1.81 g (66%) of 1,6-dideoxy-2,3,4-tri-O-pivaloyl-1-(phenylsulfinyl)-β-L-galactopyranose 5 as a mixture of diastereomers: Rf 0.05 and 0.13 (15% EtOAc/petroleum ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040433
Source datasetuspto-grants-2000_03
ORD IDord-351b3ca97e8441ab9d890faab6b5470b
Source noteuspto-grants-2000_03