HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643242Generated: October 26, 2026
Dimethylformamide → 3-Chloro-5-methoxybenzaldehyde
https://huagongshe.com/reaction/643242
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3,5-Dichloroanisole | HCID 36588 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | 1,2-Dibromoethane | HCID 7839 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloro-5-methoxybenzaldehyde | HCID 21904633 | 54% |
Reaction Steps
3,5-Dichloroanisole (74.0 g, 419 mmol) in THF (200 mL) was added dropwise to magnesium metal (14.2 g, 585 mmol, pre-washed with 0.5 N HCl) in THF (100 mL) at 25° C. After the addition, 1,2-dibromoethane (3.9 g, 20.8 mmol) was added dropwise. The resultant dark brown mixture was heated at reflux for 3 h. The mixture was cooled to 0° C., and N,N-dimethylformamide (60 mL) was added in one portion. The mixture was partitioned with diethyl ether (3×400 mL) and 6N HCl (500 mL). The combined organic extracts were washed with brine (300 mL), dried (Na2SO4), filtered and concentrated in vacuo to give an oil. Flash chromatography (2×) on silica gel eluting with Hex:EtOAc (4:1) afforded the sub-title compound (38.9 g, 54%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700582B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-362ceedd52634e999dc8f00569535921 |
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| Source note | uspto-grants-2010_04 |
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