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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037080Generated: October 31, 2026

Dimethylformamide → Ethyl 8-formylindolizine-5-carboxylate

https://huagongshe.com/reaction/1037080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylsilaneHCID 12052—
ReactantEthyl 8-(((trifluoromethyl)sulfonyl)oxy)indolizine-5-carboxylateHCID 86685512—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
ProductEthyl 8-formylindolizine-5-carboxylateHCID 8668551939%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 8-(((trifluoromethyl)sulfonyl)oxy)indolizine-5-carboxylate (4 g, 11.87 mmol) in DMF (1200 mL) was added TEA (3.6 g, 35.61 mmol), Et3SiH (4.14 g, 35.61 mmol) and Pd(dppf)2Cl2 (0.9 g, 10 mol %) under N2. The reaction mixture was stirred at 60° C. under CO (50 psi) overnight. The mixture was concentrated and to the residue were added EA and water, washed with brine, dried and concentrated and purified by column to give product ethyl 8-formylindolizine-5-carboxylate (1 g, yield 39%). 1H NMR (400 MHz, DMSO-d6): δ 10.15 (s, 1H), 8.61 (s, 1H), 7.76 (m, 1H), 7.63 (m, 1H), 7.37 (m, 1H), 7.10 (m, 1H), 4.46 (q, 2H), 1.39 (t, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546357B2
Source datasetuspto-grants-2013_10
ORD IDord-0286f9f51638497b9363d15aa042d32a
Source noteuspto-grants-2013_10