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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291922Generated: November 1, 2026

Propargyl bromide → HCID 13605018, compound

https://huagongshe.com/reaction/2291922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21278472HCID 21278472—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13605018HCID 1360501876.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

826 mg of 3-nitro-1H-pyrrole-4-carboxaldehyde [prepared by the process in Bull. Soc. Chim. p. 283-29 (1972)] were poured into 40 ml of tetrahydrofuran and then, at +5° C., 280 mg of sodium hydride as 50% in oil were added. After leaving the temperature at 20° C. for one hour, 1.19 g of propargyl bromide were added. The mixture was stirred for 18 hours at 20° C. and then was filtered and concentrated. The residue was chromatographed over silica and eluted with a mixture of hexane and ethyl acetate (1-1) to obtain 800 mg of 3-nitro-1-(2-propynyl) 1H-pyrrol-4-carboxaldehyde melting at 120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04798901
Source datasetuspto-grants-1989_01
ORD IDord-76d2ca65b20f4c31870103d1b6087b2d
Source noteuspto-grants-1989_01