HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169980Generated: October 28, 2026
2,3-Dimethylbenzaldehyde → HCID 44815677, compound
https://huagongshe.com/reaction/1169980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dimethylbenzaldehyde | HCID 34224 | — |
| Reactant | 1-(diethoxymethyl)-1H-imidazole | HCID 3849535 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 44815677 | HCID 44815677 | 72% |
Reaction Steps
To a solution of 1-(diethoxymethyl)-1H-imidazole (698 mg, 4.10 mmol) in anhydrous tetrahydrofuran (7 ml), at −78° C., was added n-butyllithium (2.5 M in hexane, 1.64 ml, 4.1 mmol). The reaction mixture was stirred at −78° C. for 1 h, before addition of a solution of 2,3-dimethylbenzaldehyde (500 mg, 3.73 mmol) in tetrahydrofuran (3 ml). The reaction mixture was stirred at −78° C. for 2 h, warmed to room temperature and quenched with ice cold hydrochloric acid (4M, 20 ml). The reaction mixture was concentrated in vacuo and to the residue was added water (20 ml). The solution was extracted with diethyl ether (2×20 ml) and the aqueous layer was basified by addition of solid sodium hydrogen carbonate. This solution was extracted with ethyl acetate (3×20 ml) and the combined organic phases were dried (MgSO4) and concentrated in vacuo to give the title compound (543 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825149B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-7c544e14b83a44cf8609940d8357913c |
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| Source note | uspto-grants-2010_11 |
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