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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948296Generated: October 30, 2026

Sodium Hydroxide → ethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1948296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantChlorosuccinimideHCID 31398—
Reactant3,4-Dichloro-5-methyl-1H-pyrrole-2-carboxylic acidHCID 25137682—
SolventChloroformHCID 6212—
Productethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylateHCID 6670718938%

Reaction Conditions

Temperature40 °C

Reaction Steps

N-Chlorosuccinimide (0.67 g, 5.08 mmol) was added to a solution of ethyl 5 -methyl-1H-pyrrole-2-carboxylate (Intermediate 3; 0.65 g, 4.23 mmol) in chloroform (20 ml). The reaction was warmed to 40° C. and stirred for 4 h, then poured to a beaker containing 2 N NaOH (20 ml) at 0° C. The layers were separated and the aqueous layer was extracted with chloroform (×3). The combined organic extracts were dried over magnesium sulfate and concentrated. The resultant off-white solid was purified by flash chromatography (hexanes/EtOAc, 16:1) to give the title product as a white solid (0.3 g, 38%). MS (ES): 188 (M+1) for C8H10ClNO2; NMR (CDCl3): 1.34 (t, 3H), 2.27 (s, 3H), 4.30 (q, 2H), 6.76 (s, 1H), 9.07 (brs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399489B2
Source datasetuspto-grants-2013_03
ORD IDord-239c79f6d7d74639a67b0d4942d5c76d
Source noteuspto-grants-2013_03