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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655752Generated: October 27, 2026

Triethylamine → ethyl 3-bromo-4-chloro-5-methyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/655752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantSodium BisulfiteHCID 23665763—
Reactantethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylateHCID 66707189—
SolventDichloromethaneHCID 6344—
Productethyl 3-bromo-4-chloro-5-methyl-1H-pyrrole-2-carboxylateHCID 66707680106.2%

Reaction Steps

Bromine (0.56 ml, 11 mmol) was added to a solution of 1 g (5.3 mmol) of ethyl 4-chloro-5-methyl-1H-pyrrole-2-carboxylate (WO2006087543) and 0.8 ml (5.7 mmol) Et3N in CH2Cl2. After stirring at room temperature for 2 h, aqueous NaHSO3 was added and the CH2Cl2 was removed and the aqueous residue was partitioned between water and EtOAc. The EtOAc layer was separated and washed with brine. The EtOAc layer was dried over anhydrous MgSO4, and the solvent was removed to give 1.5 g of the product as a solid. MS (ES) (MH+): 240 for C8H9BrClNO2; NMR (d6-DMSO): 1.3 (t, 3H), 2.2 (s, 3H), 4.2 (q, 2H), 12.3 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071605B2
Source datasetuspto-grants-2011_12
ORD IDord-f8c919a1364e42e788a071f2188cd9ef
Source noteuspto-grants-2011_12