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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247473Generated: November 2, 2026

Dimethyl Sulfoxide → (1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)-acetaldehyde

https://huagongshe.com/reaction/1247473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDichloromethaneHCID 6344—
ReactantSulfur trioxide-pyridineHCID 168533—
Reactant2-(1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)-ethanolHCID 10891051—
SolventWaterHCID 962—
Product(1,8-Diethyl-1,3,4,9-tetrahydropyrano[3,4-b]indol-1-yl)-acetaldehydeHCID 2051614952%

Reaction Steps

To a stirred solution of compound 1 (136 mg, 0.5 mmol), CH2Cl2 (2 mL), dry DMSO (142 μL, 2.0 mmol, 4.0 eq), and dry TEA (697 μL, 5.0 mmol, 10.0 eq) at room temperature under argon, sulfur trioxide-pyridine complex (Pyr-SO3, 318 mg, 2.0 mmol, 4.0 eq) was added in a portion-wise manner and stirred for two days. The resulting mixture was then diluted with water and extracted three times with Et2O. The combined organic phases were dried with Na2SO4, concentrated, and purified by column chromatography using 20:80:EtOAc:Hexane to give a yellow-white solid (70 mg, 52%). Spectral data were identical to those reported above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129262B2
Source datasetuspto-grants-2006_10
ORD IDord-6cb39121d99a48b69a0dce1db6f94542
Source noteuspto-grants-2006_10