HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368549Generated: October 29, 2026
Dimethylformamide → HCID 178488618, compound
https://huagongshe.com/reaction/1368549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 18520211 | HCID 18520211 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178488618 | HCID 178488618 | — |
Reaction Steps
Production of 3,5-Dimethyl-4-methoxybenzaldehyde 5-Bromo-1,3-dimethyl-2-methoxybenzene (70.10 g) was dissolved in THF (700 ml). The solution was cooled to −78° C. To the reaction mixture was added dropwise n-butyl lithium in hexane (1.62 M, 250 ml), and the mixture was stirred for 15 min. To the mixture was added DMF (50 ml), and the temperature of the mixture was elevated to 0° C. To the reaction mixture was added an aqueous solution of ammonium chloride and ethyl acetate, and the mixture was extracted with ethyl acetate. The organic layer was dried and concentrated. To the residue was added ethyl acetate. The organic layer was washed with water and saturated solution of sodium chloride, dried and concentrated to give the titled compound (52.80 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06573289B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-d2ee6e9a0be1441e8055d04740123814 |
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| Source note | uspto-grants-2003_06 |
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