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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072192Generated: October 30, 2026

Water → 3-(5-Formyl-4-methyl-1H-pyrrol-2-yl)propanoic acid

https://huagongshe.com/reaction/1072192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 22390964HCID 22390964—
SolventTrifluoroacetic acidHCID 6422—
Product3-(5-Formyl-4-methyl-1H-pyrrol-2-yl)propanoic acidHCID 22390993100.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-(2-carboxy-ethyl)-3-methyl-1H-pyrrole-2-carboxylic acid (1.3 g, 6.59 mmol) in trifluoroacetic acid (6 mL) was stirred at room temperature for 10 minutes. It was then cooled to 0° C. and to it was added triethyl orthoformate (6 mL). The mixture was stirred at 0° C. for 10 minutes and at room temperature for 10 minutes. The reaction was poured into water (50 mL) and extracted with ethyl acetate. The extract was dried and concentrated to give 1.2 g of 3-(5-formyl-4-methyl-1H-pyrrol-2-yl)-propionic acid as a brown solid. 1H NMR (300 MHz, DMSO-d6) δ 12.17 (br s, 1H), 11.50 (br s, 1H), 9.44 (s, 1H, CHO), 5.85 (s, 1H), 2.74 (t, J=7.4 Hz, 2H, CH2), 2.54 (t, J=7.4 Hz, 2H, CH2), 2.23 (s, 3H, CH3). MS 182 [M++1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908930B2
Source datasetuspto-grants-2005_06
ORD IDord-9b65b88ab32e497b9a36ff24a2f91519
Source noteuspto-grants-2005_06