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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Thiazole-5-carbaldehyde | HCID 2773577 | — |
| Reactant | HCID 178419672 | HCID 178419672 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22013962 | HCID 22013962 | 58.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204293B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-686d227bda764e72875772395e37a0d5 |
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| Source note | uspto-grants-2001_03 |
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