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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635981Generated: October 26, 2026

3-Bromo-4-fluorobenzaldehyde → methyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylate

https://huagongshe.com/reaction/635981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
Reactant2H-pyran-3,5(4H,6H)-dioneHCID 325287—
ReactantMethyl 3-aminocrotonateHCID 643918—
SolventEthanolHCID 702—
Productmethyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylateHCID 1125796450.5%

Reaction Steps

A mixture of tetrahydropyran-3,5-dione (Terasawa, J. Org. Chem. (1977), 42, 1163-1169) (1.4 g, 12 mmol), 3-bromo-4-fluorobenzaldehyde (3.0 g, 15 mmol), methyl 3-aminocrotonate (1.4 g, 12 mmol) and ethyl alcohol (10 mL) was processed as described in Example 2A. Purification by flash chromatography over silica gel (1% then 2% and then 5% methyl alcohol/methylene chloride) provided the title compound (2.4 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06191140B1
Source datasetuspto-grants-2001_02
ORD IDord-1d95bf639658426e918c34609308f604
Source noteuspto-grants-2001_02