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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41701Generated: October 25, 2026

Ethyl Acetate → 4-[4-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/41701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant8-(4-Bromophenyl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 12169341—
ReactantTert-butyl 1,2,3,4-tetrahydroquinoxaline-1-carboxylateHCID 16740533—
ReactantSodium t-butoxideHCID 23676156—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
Product4-[4-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl esterHCID 6686317458.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

0.31 g of 8-(4-bromophenyl)-1,4-dioxa-8-azaspiro[4.5]decane is placed in 5 ml of anhydrous o-xylene. 0.24 g of 3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester is added, then 0.15 g of sodium tert-butoxide is added, followed by 0.009 g of palladium acetate, and then the addition is completed with 0.0084 g of tri(tert-butyl)phosphine. The reaction mixture is heated at 150° C. for 4 h, then the heating is halted and the mixture is brought back to ambient temperature. Ethyl acetate is added and the mixture is washed twice with water and then twice with a saturated aqueous sodium chloride solution. The organic phase is dried over sodium sulphate and concentrated under reduced pressure. The crude product obtained is chromatographed on silica gel, elution being carried out with a heptane/ethyl acetate (4/1) solvent mixture. 0.27 g of 4-[4-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)phenyl]-3,4-dihydro-2H-quinoxaline-1-carboxylic acid tert-butyl ester is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530657B2
Source datasetuspto-grants-2013_09
ORD IDord-a8f50c093ac846ea8b461c27c1bae8f6
Source noteuspto-grants-2013_09