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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792254Generated: November 1, 2026

Toluene → HCID 178424531, compound

https://huagongshe.com/reaction/1792254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant2,2-DimethoxypropaneHCID 6495—
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 22034120HCID 22034120—
ProductHCID 178424531HCID 178424531—

Reaction Steps

To a solution of 2-ethyl 2-amino-1-(2,4,6-trimethylphenyl)indolizine-3-carboxylate (19.2 g; 59.6 mmol) in 2,2-dimethoxypropane (100 mL), add dl-camphorsulfonic acid (0.2 g). Stir the mixture at reflux for 30 min and then distill slowly to remove ca. 60 mL of volatiles over a 30-minute period. Cool the solution to ambient temperature under inert atmosphere, dilute with anhydrous toluene (50 mL), and concentrate in vacuo. Dissolve the residue in toluene (50 mL) and add dropwise over a 1-hour period a 0.5 M solution of potassium bis(trimethylsilyl)amide in toluene (250 mL; 125 mmol) to the stirred solution. After the addition, stir the mixture for 2 h at ambient temperature, concentrate in vacuo to a small volume and dilute with aqueous NH4Cl. Filter the resulting biphasic mixture and wash successively with water, MeOH, and Et2O. Dry under vacuum to obtain the title compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074929B2
Source datasetuspto-grants-2006_07
ORD IDord-44429aaa5f9c4912afa90daad3429515
Source noteuspto-grants-2006_07