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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532865Generated: October 30, 2026

1,3-Thiazole-5-carbaldehyde → HCID 22013962, compound

https://huagongshe.com/reaction/1532865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Thiazole-5-carbaldehydeHCID 2773577—
ReactantHCID 178419672HCID 178419672—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22013962HCID 2201396258.5%

Reaction Steps

A solution of thiazole-5-carboxaldehyde (2.31 g, 20.4 mmol) in 20 mL of in THF was added to a cold (0° C.) solution of 2-cyclohexylethylmagnesium bromide (prepared from 2-bromoethylcyclohexane (7.88 g) and magnesium turnings (1.22 g)) in 30 mL of ethyl ether and the mixture stirred 30 minutes. The cold bath was removed and the mixture stirred for 2 hours more and then quenched by the addition of 3N aqueous HCl. The solution was stirred until 2 clear phases resulted and then the layers were separated. The pH of the aqueous phase was adjusted to 4 with 2M aqueous sodium carbonate and then extracted with 3 portions of ethyl acetate. All the organic phases were combined and washed with brine, dried, filtered and concentrated. The residue was purified by column chromatography on silica gel (125 g, 50% ethyl acetate/hexanes) to provide 2.69 g (58%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204293B1
Source datasetuspto-grants-2001_03
ORD IDord-686d227bda764e72875772395e37a0d5
Source noteuspto-grants-2001_03