HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218093Generated: October 26, 2026
2-fluoro-N,3-dimethoxy-N-methylbenzamide → 2-Fluoro-3-methoxybenzaldehyde
https://huagongshe.com/reaction/2218093
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-fluoro-N,3-dimethoxy-N-methylbenzamide | HCID 17981929 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluoro-3-methoxybenzaldehyde | HCID 3774463 | 85% |
Reaction Steps
To a solution of 2-fluoro-3,N-dimethoxy-N-methyl-benzamide (2.30 g, 10.8 mmol) in THF (20 mL) at −78° C. was added 1M DEBAL-H in toluene.(12 mL, 12 mmol). The reaction stirred at −78° C. for 3 h and then the remaining 1M DIDAL-H in toluene (4.2 mL, 4.2 mmol) was added to the reaction. The reaction was allowed to stir at −78° C. for 30 min and was then warmed to rt. The reaction was quenched slowly with saturated aqueous NH4Cl. The organic phase was separated and the aqueous phase was extracted with 2×50 mL ethyl acetate. The combined organic phases were washed successively with 1N HCl and brine. The organic phase was dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography eluting silica gel with EtOAc:hexane [0:100 to 1:1] to yield the title compound (1.41 g, 85%): δH (300 MHz, CDCl3): 10.38 (1H, s), 7.43-7.40 (1H, m), 7.24-7.15 (2H, m), 3.95 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07410982B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-7c7e92e8c78a4ad8abe2a84d170b9a94 |
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| Source note | uspto-grants-2008_08 |
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