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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189531Generated: November 2, 2026

Sodium Bicarbonate → ethyl 2-(2-cyclohexyl-5-methyl-1H-pyrrol-1-yl)acetate

https://huagongshe.com/reaction/1189531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant1-Cyclohexylpentane-1,4-dioneHCID 12394855—
SolventDichloromethaneHCID 6344—
Productethyl 2-(2-cyclohexyl-5-methyl-1H-pyrrol-1-yl)acetateHCID 6723799780.4%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of 1-cyclohexylpentane-1,4-dione (1.32 g, 7.24 mmol) in dichloromethane (10 mL) was added ethyl 2-aminoacetate hydrochloride (1.01 g, 7.24 mmol) and solid sodium bicarbonate (1.52 g, 18.1 mmol). The reaction was heated at 55° C. for 6 hours, then stirred at 40° C. for an additional 14 hours, after which the reaction was nearly complete by LCMS analysis. The reaction mixture was cooled to room temperature, extracted with dichloromethane (3×50 mL), dried (sodium sulfate), filtered, and concentrated to a brown residue. Purification by silica gel column chromatography (Luknova 80 g, 20 mL/min) using 0 to 35% ethyl acetate in hexanes over 50 minutes afforded the product as a clear, colorless oil (1.45 g, 5.82 mmol, 80% yield). 1H NMR (400 MHz, CDCl3): δ (ppm) 5.86 (dd, 1H), 5.83 (d, 1H), 4.53 (s, 2H), 4.24 (q, 2H), 2.33 (m, 1H), 2.17 (d, 3H), 1.71-1.89 (m, 5H), 1.32-1.42 (m, 5H), 1.29 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674115B2
Source datasetuspto-grants-2014_03
ORD IDord-b4a383768f194e198d4718dbc4c4a441
Source noteuspto-grants-2014_03