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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532826Generated: October 30, 2026

Morpholine → 2-(Morpholin-4-yl)-1,3-thiazole-4-carbaldehyde

https://huagongshe.com/reaction/532826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantEthyl AcetateHCID 8857—
Reactant2-Bromo-1,3-thiazole-4-carboxaldehydeHCID 17750433—
ReactantEthyl acetate hexaneHCID 21226206—
Solvent1,4-DioxaneHCID 31275—
Product2-(Morpholin-4-yl)-1,3-thiazole-4-carbaldehydeHCID 1505357975.5%

Reaction Steps

To a slurry of 2-bromothiazole-4-carbaldehyde (1.0 g, 5.21 mmol) in p-dioxane (5 mL) was added morpholine (1.36 g, 15.61 mmol) over 1 min. The mixture was heated to 100° C. for 1 h (monitored by TLC, EtOAc/hexane 1:1) and cooled to room temperature. EtOAc (20 mL) was added and the solid residue filtered off and washed with EtOAc (30 mL). The combined organic layer was washed with brine (30 mL) and concentrated. The residue was purified by silica gel flash column chromatography using 20 to 75% EtOAc in hexane to afford the title compound as a light tan solid (780 mg, 75%): 1H NMR (400 MHz, CDCl3) δ 9.70 (s, 1H), 7.49 (s, 1H), 3.82 (t, 41-1, J=4.8 Hz), 3.56 (t, 4H, J=4.8 Hz). MS (ES) m/z 199.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853202B2
Source datasetuspto-grants-2014_10
ORD IDord-8219d29ea1464a0daea3e2e7636d7c7b
Source noteuspto-grants-2014_10