HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629427Generated: October 30, 2026
Thionyl Chloride → 4-(chloromethyl)-2-fluoro-N-methylbenzamide
https://huagongshe.com/reaction/629427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-fluoro-4-(hydroxymethyl)-N-methylbenzamide | HCID 117977065 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(chloromethyl)-2-fluoro-N-methylbenzamide | HCID 117977084 | — |
Reaction Steps
To a solution of 2-fluoro-4-(hydroxymethyl)-N-methylbenzamide (2.11 g) in THF (46.1 mL) was added dropwise thionyl chloride (1.01 mL) under ice-cooling, and the mixture was stirred overnight at room temperature. To the reaction solution was added saturated aqueous sodium bicarbonate, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate/hexane). The objective fractions were collected, and washed with diisopropyl ether, and the precipitate was collected by filtration. The filtrate was concentrated, and the residue was washed with diisopropyl ether. This procedure was repeated three times to give the title compound (0.96 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315458B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-49c2b28852ee465d81d508a1fc4d3447 |
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| Source note | uspto-grants-2016_04 |
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