HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169961Generated: October 29, 2026
N,N,N',N'-Tetramethylethylenediamine → HCID 67081945, compound
https://huagongshe.com/reaction/1169961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 2',3'-Dimethylacetophenone | HCID 16505 | — |
| Reactant | 1-(diethoxymethyl)-1H-imidazole | HCID 3849535 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Product | HCID 67081945 | HCID 67081945 | 76.1% |
Reaction Steps
1-(Diethoxymethyl)imidazole (76.0 g, 446 mmol) and N,N,N,N-tetramethylethylene diamine (67.6 mL, 446 mmol) were dissolved in 2-methyltetrahydrofuran (400 ml) and cooled to −40° C., under nitrogen. n-Butyl lithium (2.5M in hexane, 180 ml, 446 mmol) was added slowly maintaining the reaction temperature at <−25° C. throughout. The reaction mixture was stirred for an hour and allowed to warm to 0° C., after which 2,3-dimethylacetophenone (44.00 g, 297.00 mmol) was added whilst maintaining the reaction temperature at <15° C. throughout. The reaction was stirred at room temperature overnight and then quenched with aqueous hydrochloric acid (2N, 1 l). The mixture was extracted with ethyl acetate (500 ml) and to the aqueous layer was added sodium carbonate. The aqueous layer was further extracted with ethyl acetate (800 ml) and the combined extracts were washed with water (500 ml), dried (MgSO4) and concentrated in vacuo to give the title compound (48.9 g).
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-ccaeb6e84c914d33be60646594be2fb6 |
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| Source note | uspto-grants-2010_11 |
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