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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331044Generated: October 30, 2026

Acetone cardice → 2-(6-bromo-5-fluoro-1H-indol-1-yl)ethanol

https://huagongshe.com/reaction/331044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetone cardiceHCID 18522661—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 2-(6-bromo-5-fluoro-1H-indol-1-yl)acetateHCID 71090281—
SolventTetrahydrofuranHCID 8028—
Product2-(6-bromo-5-fluoro-1H-indol-1-yl)ethanolHCID 7109040596.1%

Reaction Steps

Methyl 2-(6-bromo-5-fluoro-1H-indol-1-yl)acetate (D77) (10.2 g, 35.7 mmol) was dissolved up in 81 mL of THF and cooled in a cardice/acetone bath before the addition of LiAlH4 (2N in THF solution) (17.83 mL, 35.7 mmol). The reaction mixture was left to stir in the cardice/acetone bath for 30 mins. Whilst still in the bath the reaction mixture was quenched by the dropwise addition of saturated sodium sulfate aqueous solution. The solid formed was filtered off and washed with ethyl acetate. The filtrate was washed with brine. The organic layer was passed through a hydrophobic frit and concentrated to afford title compound (8.852 g). LCMS (A): m/z (M+H)+ 258/260, C10H9BrFNO requires 257/259 (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877742B2
Source datasetuspto-grants-2014_11
ORD IDord-94067bdb7f104c4787aaec2c082cac26
Source noteuspto-grants-2014_11