HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220293Generated: October 29, 2026
Dimethyl Sulfate → 3-Fluoro-2-methoxybenzaldehyde
https://huagongshe.com/reaction/2220293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Fluorosalicylaldehyde | HCID 587788 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Fluoro-2-methoxybenzaldehyde | HCID 12572277 | 100% |
Reaction Steps
To a suspension of 3-fluoro-2-hydroxybenzaldehyde (5.328 g, 38.02 mmol) and potassium carbonate (7.88 g, 57.03 mmol) in acetone (60 mL) was added dimethyl sulphate (3.96 mL, 41.83 mmol). The resulting suspension was stirred at 60° C. for 2 h before being allowed to cool and then concentrated in vacuo. The residue was dissolved in dichloromethane (100 mL) and water (50 mL). The organic phase was washed with saturated sodium bicarbonate (50 mL) with the resulting organic phase being dried (MgSO4) and the solvent evaporated in vacuo to give a pale yellow oil (6.262 g, 38.02 mmol, 100%). δH (300 MHz, CDCl3) 10.40 (1H, s, CHO), 7.60 (1H, d, Ar), 7.30 (1H, m, Ar), 7.10 (1H, m, Ar), 4.10 (3H, s, OCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07417064B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-e4212303d20049d2a3a619eef1968de6 |
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| Source note | uspto-grants-2008_08 |
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