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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299262Generated: October 30, 2026

Toluene → HCID 178424432, compound

https://huagongshe.com/reaction/2299262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 22034120HCID 22034120—
Solvent2,2-DimethoxypropaneHCID 6495—
ProductHCID 178424432HCID 17842443254%

Reaction Steps

To a solution of 2-amino-3-ethoxycarbonyl-1-(2,4,6-trimethylphenyl)-indolizine (19.2 g; 59.6 mmol) in 2,2-dimethoxypropane (100 mL) is added di-camphorsulfonic acid (0.2 g). The mixture is stirred at reflux for 30 minutes and then distilled slowly to remove ca. 60 mL of volatiles over a 30-minute period. The solution is cooled to ambient temperature under an inert atmosphere, diluted with anhydrous toluene (50 mL), and concentrated in vacuo. The residue is dissolved in toluene (50 mL) and to the stirred solution is then added a 0.5 M solution of potassium bis(trimethylsilyl)amide in toluene (250 mL; 125 mmol) dropwise over a 1-hour period. After the addition is complete, the mixture is further stirred for 2 hours at room temperature before being concentrated in vacuo to a small volume and then diluted with aqueous ammonium chloride. The resulting emulsion-like biphasic mixture is suction-filtered and washed succesively with water, methanol, and ethyl ether. Air- and vacuum drying provides 10.1 g of the title compound as a pale yellow solid (54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495686B2
Source datasetuspto-grants-2002_12
ORD IDord-8674363f345c4885859d52987c9040ce
Source noteuspto-grants-2002_12