HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473235Generated: October 31, 2026
(Diethylamino)sulfur trifluoride → Dimethyl 5-fluoromethylisophthalate
https://huagongshe.com/reaction/473235
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Dimethyl 5-(hydroxymethyl)isophthalate | HCID 13907324 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dimethyl 5-fluoromethylisophthalate | HCID 67254949 | 78% |
Reaction Steps
Under Ar atmosphere, with ice-cooled, to a solution of dimethyl 5-hydroxymethylisophthalate (32) (3.36 g, 15.0 mmol) in CH2Cl2 (150 mL, 0.1 M solution) was slowly added dropwise (diethylamino)sulfur trifluoride (4.00 mL, 30.5 mmol), and stirred for 2 hours at a room temperature. TLC was used to confirm the progress of the reaction. Then, the reaction was quenched with MeOH (150 mL). The solvent was removed under reduced pressure. The residue was subjected to extraction with EtOAc and a saturated sodium hydrogen carbonate aqueous solution (three times). The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate, and evaporated under reduced pressure to remove the solvent. The residue was purified by neutral silica gel column chromatography (hexane:EtOAc=10:1) to isolate dimethyl 5-fluoromethylisophthalate (33) (2.57 g, 78%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633304B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-f8ba0628382f48d48f715655aed4e2c2 |
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| Source note | uspto-grants-2014_01 |
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