HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037080Generated: October 31, 2026
Dimethylformamide → Ethyl 8-formylindolizine-5-carboxylate
https://huagongshe.com/reaction/1037080
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Ethyl 8-(((trifluoromethyl)sulfonyl)oxy)indolizine-5-carboxylate | HCID 86685512 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Product | Ethyl 8-formylindolizine-5-carboxylate | HCID 86685519 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546357B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-0286f9f51638497b9363d15aa042d32a |
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| Source note | uspto-grants-2013_10 |
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