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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037067Generated: October 30, 2026

Methyl 5-(hydroxymethyl)indolizine-8-carboxylate → Methyl 5-formylindolizine-8-carboxylate

https://huagongshe.com/reaction/1037067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(hydroxymethyl)indolizine-8-carboxylateHCID 86685514—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-formylindolizine-8-carboxylateHCID 8668551345%

Reaction Steps

To a solution of methyl 5-(hydroxymethyl)indolizine-8-carboxylate (13 g, 63.41 mmol) in DCM (300 mL) was added MnO2 (55 g, 0.634 mol) at 0° C. The reaction mixture was stirred at rt overnight. After the completion, the reaction was filtered and concentrated. The crude product was purified by column (PE:EtOAc=300:1) to give the desired product methyl 5-formylindolizine-8-carboxylate (5.8 g, yield 45%). 1H NMR (400 MHz, DMSO): δ 10.01 (s, 1H), 8.90-8.91 (m, 1H), 7.31-7.35 (d, 1H, J=7.6 Hz), 7.68-7.70 (d, 1H, J=1 Hz), 7.29-7.31 (m, 1H), 7.14-7.16 (m, 1H), 3.97 (s, 3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546357B2
Source datasetuspto-grants-2013_10
ORD IDord-7ac2aa5f036548a49264935e2579b58a
Source noteuspto-grants-2013_10