HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881864Generated: November 1, 2026
Citric Acid → 4-(2,2-Dimethyl-1,3-dioxolan-4-yl)-1,3-thiazole-2-carbaldehyde
https://huagongshe.com/reaction/1881864
Participants
| Role | Name | HCID | Charge |
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| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 59331272 | HCID 59331272 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2,2-Dimethyl-1,3-dioxolan-4-yl)-1,3-thiazole-2-carbaldehyde | HCID 59331237 | 42.5% |
Reaction Steps
To a solution of 2-bromo-4-(2,2-dimethyl-1,3-dioxolan-4-yl)-1,3-thiazole (3.00 g) in tetrahydrofuran (40 mL) was slowly added a 1.6M n-butyllithium hexane solution (7.8 mL) at −70° C. under a nitrogen atmosphere. The reaction mixture was stirred at −70° C. for 1 hr, and N,N-dimethylformamide (2.50 g) was added. The reaction mixture was warmed to room temperature, 10% aqueous citric acid solution was added, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography, and the title compound (1.03 g, yield 42%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (1:5, volume ratio).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318746B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-ece59b52b32f44a6adfd9d0b481cddee |
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| Source note | uspto-grants-2012_11 |
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