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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939252Generated: October 25, 2026

1,3-Dibromopropane → ethyl 3,4-dihydro-2H-pyrano[2,3-b]indolizine-10-carboxylate

https://huagongshe.com/reaction/1939252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium HydroxideHCID 14797—
Reactant1,2-Di-[(ethoxycarbonyl)methyl]pyridinium bromideHCID 21467252—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Productethyl 3,4-dihydro-2H-pyrano[2,3-b]indolizine-10-carboxylateHCID 21467249—

Reaction Steps

A solution of 1,2-di-[(ethoxycarbonyl)methyl]pyridinium bromide (1.5 g, 0.0045 mole) and 1,3-dibromopropane (0.45 ml, 0.0045 mole) in ethanol (10 ml) was added over 5 minutes to a stirred solution of potassium hydroxide (0.75 g, 0.0134 mole) in ethanol (15 ml) at 5° C. The mixture was then allowed to warm upto room temperature and stir for 20 h. The reaction mixture was diluted with water (150 ml) and extracted with ethyl acetate (2×100 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to leave a brown oil. This was chromatographed on silica gel eluting with ether to afford the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05696129
Source datasetuspto-grants-1997_12
ORD IDord-e9e59f44f0d042cb8141c696d02a6c4e
Source noteuspto-grants-1997_12