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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204294Generated: October 31, 2026

2-formyl-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl ester → 2-[(4-chloro-2-methyl-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2204294

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-formyl-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 86703097—
ReactantHCID 178426105HCID 178426105—
SolventTetrahydrofuranHCID 8028—
Product2-[(4-chloro-2-methyl-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 86703096—

Reaction Steps

A solution (0.5 M in THF) of 4-chloro-2-methylphenylmagnesium bromide [480438-47-9] (68.8 mmol) was added to a mixture of 2-formyl-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl ester (Step A5) (68.8 mmol) in THF (160 mL) at 0° C. After stirring for 2 h, the reaction mixture was quenched with a saturated aqueous solution of NH4Cl and extracted with MTBE (2×). The combined organic phases were successively washed with water and brine, dried (Na2SO4), filtered and concentrated. The residue was suspended in hexanes, stirred for 30 min and then filtered to afford the title compound as a white solid. tR: 7.74 min (HPLC 2); ESI-MS: tR=1.26 min, [M]+318/320 (i.e. fragmented pyrrolium ion) (LC-MS 1); TLC: Rf=0.20 (1:6 EtOAc/hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-2d103459bf6e4d4cb11e9af0d68184b6
Source noteuspto-grants-2016_06