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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389899Generated: October 31, 2026

3-[4-(Trimethylsilyl)-2,3-dihydrofuro[2,3-b]pyridin-5-yl]propanal → 1,6,7,8-tetrahydro-2H-cyclopenta[d]furo[2,3-b]pyridin-8-ol

https://huagongshe.com/reaction/2389899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[4-(Trimethylsilyl)-2,3-dihydrofuro[2,3-b]pyridin-5-yl]propanalHCID 59179448—
CatalystTetrabutylammonium DifluorotriphenylsilicateHCID 9893474—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventAmmonium ChlorideHCID 25517—
Product1,6,7,8-tetrahydro-2H-cyclopenta[d]furo[2,3-b]pyridin-8-olHCID 5917937171%

Reaction Steps

To a solution of tetrabutylammonium difluorotriphenylsilicate (43.3 mg, 0.802 mmol) in 1,2-dimethoxyethane (3 mL) heated to 70° C. was added dropwise a solution of 3-[4-(trimethylsilyl)-2,3-dihydrofuro[2,3-b]pyridin-5-yl]propanal (100 mg, 0.401 mmol) in 1,2-dimethoxyethane (1 mL). After dropwise addition, the reaction solution was diluted with saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=30/70→100/0) to give the title compound (50.4 mg, yield 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273761B2
Source datasetuspto-grants-2012_09
ORD IDord-feafff4fb6af4b6d836378bd911684a0
Source noteuspto-grants-2012_09