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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175658Generated: October 31, 2026

Triethylamine → 3-[4-(Methansulfonylmethyl)phenoxy]phthalonitrile

https://huagongshe.com/reaction/1175658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(4-(Hydroxymethyl)phenoxy)phthalonitrileHCID 53439489—
SolventDichloromethaneHCID 6344—
Product3-[4-(Methansulfonylmethyl)phenoxy]phthalonitrileHCID 1125540893%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-[4-(hydroxymethyl)phenoxy]phthalonitrile (900 mg, 3.9 mmol) prepared according to procedures described in literature, and triethylamine (0.75 ml, 5.8 mmol) in anhydrous CH2Cl2 (50 ml), kept at 0° C. under stirring and in an inert atmosphere, methylsulfonylchloride was added (0.33 ml, 4.3 mmol). The mixture was stirred at 0° C. for 1 hour, then it was diluted with CH2Cl2 (50 ml) and washed with 1% HCl solution (60 ml), then with brine (50 ml), the organic layer was dried on Na2SO4 and the solvent was evaporated. 1.1 g (93%) of the title compound were obtained as a viscous fluid that crystallized on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842682B2
Source datasetuspto-grants-2010_11
ORD IDord-5345f7f1f41240ca92b0bb7b8d8d8715
Source noteuspto-grants-2010_11