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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084051Generated: November 2, 2026

Potassium hydride → HCID 10083756, compound

https://huagongshe.com/reaction/2084051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium hydrideHCID 82127—
Reactant6-BromoindoleHCID 676493—
ReactantOctahydroindolizin-7-oneHCID 11240524—
ReactantHCID 178418306HCID 178418306—
ReactantHCID 178418361HCID 178418361—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10083756HCID 10083756169%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a suspension of potassium hydride (KH; 0.289 g, 7.2 mmol) in tetrahydrofuran (THF; 5 ml) at −10° C. was added, dropwise, a solution of 6-bromoindole (1.2 g, 6 mmol) in THF (1 ml). The mixture was stirred at this temperature for 20 mins, until no more evolution of hydrogen was observed. The mixture was then cooled to −78° C. in an acetone/dry ice bath, 8.82 ml of a 1.7M solution of tBuLi was added slowly, and the mixture stirred for another 30 mins. Azabicyclo[4,3,0]nonan-4-one (1.67 g. 1.2 mmol) was then added, and the mixture stirred at −78° C. for a further 30 mins before being quenched with a mixture of dichloromethane (50 ml) and pH7 buffer (50 ml). After filtration, the organic layer was washed with water and brine, dried, concentrated, and the residue triturated with hexanes to give 0.52 g of the title product as a white powder (33.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716837B1
Source datasetuspto-grants-2004_04
ORD IDord-6555498af91f4639901d83821a110497
Source noteuspto-grants-2004_04