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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397964Generated: October 28, 2026

Oxalyl chloride → 5-(3,3,3-trifluoropropyl)-1H-pyrrole-2-carboxylic acid chloride

https://huagongshe.com/reaction/397964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant5-(3,3,3-trifluoropropyl)-1H-pyrrole-2-carboxylic acidHCID 22507269—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(3,3,3-trifluoropropyl)-1H-pyrrole-2-carboxylic acid chlorideHCID 8797717083.1%

Reaction Steps

5-(3,3,3-trifluoropropyl)-1H-pyrrole-2-carboxylic acid (5.55 mmol, 1.15 g) in CH2Cl2 (10 ml) was treated with oxalyl chloride (16.7 mmol, 1.5 ml), then DMF (1 drop). The solution was heated to reflux for 1 h, then concentrated under reduced pressure to provide 5-(3,3,3-trifluoropropyl)-1H-pyrrole-2-carboxylic acid chloride (1.04 g). 1H NMR (CDCl3) δ10.25 (1H, br s), 7.12 (1H, dd, J=4.0, 2.6), 6.12 (1H, dd, J=3.8, 2.7), 3.05-2.88 (2H, m), 2.59-2.41 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610730B2
Source datasetuspto-grants-2003_08
ORD IDord-fbe29452089d42e98c507786f7ee3141
Source noteuspto-grants-2003_08