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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515877Generated: October 30, 2026

Sulfuric Acid → Ethyl 1-methyl-2-(2-morpholinoethyl)pyrrole-3-carboxylate

https://huagongshe.com/reaction/515877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant1,1-DichloroethaneHCID 6365—
ReactantMorpholineHCID 8083—
Reactant1,4-DioxaneHCID 31275—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl 2-(2,2-diethoxyethyl)-1-methyl-pyrrole-3-carboxylateHCID 117833716—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductEthyl 1-methyl-2-(2-morpholinoethyl)pyrrole-3-carboxylateHCID 117833886—

Reaction Steps

To a solution of 3.8 g of the compound obtained in Step C (14.05 mmol) in 28 mL of tetrahydrofuran there are added 58 mL of aqueous 10% sulphuric acid solution. The reaction mixture is stirred at ambient temperature for 2 hours and then diluted with a mixture of ethyl acetate and water. After separation, the organic phase is washed with brine, dried over MgSO4 and concentrated to dryness. To a solution of the residue thereby obtained in 70 mL of dichloroethane there are added a solution of 13.5 mL of morpholine (14.5 mmol) in a mixture composed of 30 mL of dichloroethane and 3.6 mL of 4N aqueous HCL solution in dioxane (14.5 mmol), and then 7.4 g of sodium triacetoxyborohydride (NaBH(OAc)3) (35.13 mmol). The reaction mixture is stirred at ambient temperature for 3 hours and then diluted with a mixture of dichloromethane and saturated aqueous NaHCO3 solution. After separation of the phases and extraction of the aqueous phase with dichloromethane, the organic phases are dried over MgSO4 and concentrated to dryness. The crude product thereby obtained is purified by chromatography over silica gel using dichloromethane and methanol as eluants. The title product is isolated in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-4555c36905fe408c90e29a1774672b99
Source noteuspto-grants-2015_08