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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507524Generated: October 26, 2026

2-Chloro-1,3-thiazole-5-carbaldehyde → 1-(2-Chlorothiazol-5-yl)ethanone

https://huagongshe.com/reaction/507524

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-1,3-thiazole-5-carbaldehydeHCID 1479765—
ReactantHCID 178418689HCID 178418689—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Chlorothiazol-5-yl)ethanoneHCID 5177731173%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Chloro-thiazole-5-carbaldehyde (1.00 g., 6.77 mmol) was dissolved in THF (10 mL) and cooled to −78° C. MeMgBr (2.26 mL of a 3.0 M solution in Et2O, 6.78 mmol) was added dropwise. The mixture was stirred at −78° C. for 30 min and then allowed to slowly warm to −20° C. over a further 30 min. The reaction was quenched by the addition of EtOAc (2 mL), allowed to warm to 20° C., and 2 M hydrochloric acid (20 mL) was added. The mixture was poured into water (200 mL) and extracted into DCM (200 mL), dried (Na2SO4) and concentrated. The residue was dissolved in reagent grade acetone (20 mL), cooled in an ice bath, and Jones' reagent (3.0 mL of a 2.67 M solution) was added dropwise. The mixture was stirred for 16 h, allowing to warm to 20° C., and then quenched with IPA (5 mL), poured into saturated aqueous NaHCO3 (200 mL) and extracted with EtOAc (2×100 mL). The EtOAc extracts were dried (Na2SO4) and concentrated to give pure product (800 mg, 73%) as a somewhat volatile white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786132B2
Source datasetuspto-grants-2010_08
ORD IDord-3a95939a7482491a869db20a4a4ee316
Source noteuspto-grants-2010_08