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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857351Generated: November 1, 2026

Acetaldehyde → HCID 10112823, compound

https://huagongshe.com/reaction/857351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantHCID 10226143HCID 10226143—
ReactantCID 53628100HCID 178418400—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10112823HCID 10112823—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (+/−)-[8-bromo-9-[(4-chlorophenyl)sulfanyl]-6-fluoro-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl]acetic acid (Example 7, 100 mg, 0.22 mmol) in THF (4 mL) at −78° C. was added 3M MeMgBr (0.26 mmol) followed by the addition of 1.3M sec-BuLi (0.31 mmol). The reaction mixture was stirred at −78° C. for 5 minutes and an excess of acetaldehyde was added. The reaction was stirred at −78° C. for 30 minutes and quenched with saturated aqueous NH4Cl. The phases were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over Na2SO4 and concentrated. The residue was purified by silica gel chromatography eluted with EtOAc/Hexanes/AcOH (20:30:1) to provide 65 mg of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144913B2
Source datasetuspto-grants-2006_12
ORD IDord-1c0dae18d3954dc0b8e69bb0ecd61b4a
Source noteuspto-grants-2006_12