HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4347Generated: October 25, 2026
Ethyl formate → 2-Phenyl-2-[4-(4-pyridyl)-2-thiazolyl]acetaldehyde
https://huagongshe.com/reaction/4347
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl formate | HCID 8025 | — |
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 4-(2-Benzyl-1,3-thiazol-4-yl)pyridine | HCID 14096952 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Phenyl-2-[4-(4-pyridyl)-2-thiazolyl]acetaldehyde | HCID 14096956 | 39% |
Reaction Steps
To a solution of 2-benzyl-4-(4-pyridyl)thiazole (4.00 g, 0.016 mol) and tetramethylethylenediamine (2.5 mL) in dry tetrahydrofuran (35 mL) at -78° C. under nitrogen atmosphere was added dropwise n-butyl lithium (1.6M in hexane, 11.4 mL). The resulting dark mixture was allowed to stir at -78° C. for 15 minutes, warmed to 0° C. for 2 hours, then cooled to -78° C. Ethyl formate (1.47 mL) was added dropwise and the mixture allowed to stir at -78° C. for 30 minutes then at 0° C. for one hour. The reaction mixture was quenched with methanol, concentrated, and chromatographed over silica gel. Recrystallization from hexane/ethyl acetate afforded 2-phenyl-2-[4-(4-pyridyl)-2-thiazolyl]acetaldehyde (1.76 g, 39%). mp. 163°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04725606 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-18b8488c6d344783bff5729349d8b2e5 |
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| Source note | uspto-grants-1988_02 |
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