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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159761Generated: November 3, 2026

2,6-Lutidine → 1-[(2-Methoxy-5-methylphenyl)sulfonyl]indoline-4-carbaldehyde

https://huagongshe.com/reaction/1159761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantSodium periodateHCID 23667635—
Reactant1-[(2-Methoxy-5-methylphenyl)sulfonyl]-4-vinylindolineHCID 68714362—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product1-[(2-Methoxy-5-methylphenyl)sulfonyl]indoline-4-carbaldehydeHCID 86618235—

Reaction Steps

OsO4 (9 mg, 0.05 mmol) was added to a stirred mixture of 1-[(2-methoxy-5-methylphenyl)sulfonyl]-4-vinylindoline (240 mg, 0.73 mmol; Intermediate 10) and 2,6-lutidine (170 μL, 1.46 mmol) in dioxane (12 mL). The mixture turned from colorless to black in 1 minute. Sodium periodate (0.625 g, 2.92 mmol) in water (4 mL, warmed to dissolve) was added. A grey precipitation was immediately formed. The mixture was stirred for 25 min, combined with an earlier batch of this intermediate (followed this experimental and starting from Intermediate 10; 60 mg, 18 mmol), and partitioned between 2M aqueous HCl (25 mL) and DCM (25 mL). The organic layer was dried, filtered and concentrated to give the title compound (360 mg, still some dioxane according to HNMR) as a black sticky oil. MS (ESI+) for C17H17NO4S m/z 332 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812017B2
Source datasetuspto-grants-2010_10
ORD IDord-a3fa88767036422f9dc099d0ad267328
Source noteuspto-grants-2010_10