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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948347Generated: October 30, 2026

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

https://huagongshe.com/reaction/1948347

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 (Intermediate 7) 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 was separated and washed with brine. Drying (MgSO4) and removal of solvent gave 1.5 g of 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 numberUS08399489B2
Source datasetuspto-grants-2013_03
ORD IDord-526dac7ce5864486836c2638b844f95d
Source noteuspto-grants-2013_03