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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473235Generated: October 31, 2026

(Diethylamino)sulfur trifluoride → Dimethyl 5-fluoromethylisophthalate

https://huagongshe.com/reaction/473235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantDimethyl 5-(hydroxymethyl)isophthalateHCID 13907324—
SolventDichloromethaneHCID 6344—
ProductDimethyl 5-fluoromethylisophthalateHCID 6725494978%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633304B2
Source datasetuspto-grants-2014_01
ORD IDord-f8ba0628382f48d48f715655aed4e2c2
Source noteuspto-grants-2014_01