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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223760Generated: October 30, 2026

Hydrochloric Acid → 2-Cyano-4,5-diethoxy-3-fluorobenzyl methanesulfonate

https://huagongshe.com/reaction/2223760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 23093714HCID 23093714—
SolventTolueneHCID 1140—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Cyano-4,5-diethoxy-3-fluorobenzyl methanesulfonateHCID 23093715—

Reaction Conditions

Temperature8 °C

Reaction Steps

3,4-Diethoxy-2-fluoro-6-(hydroxymethyl)benzonitrile (1 g, 4.18 mmol) was dissolved in 1,2-dimethoxyethane (10 mL), and cooled in a constant temperature bath at 8° C. after addition of methanesulfonyl chloride (0.39 mL, 5.02 mmol). Triethylamine (0.76 mL, 5.43 mmol) was added dropwise to this solution at approximately 20° C. or less. After stirring at the same temperature for 1 hour, toluene (5 mL) and 0.5 N hydrochloric acid (2 mL) were added, and this was transferred to a separatory funnel and toluene (5 mL) was used for rinsing. After separation of the solution, sequential washing was carried out with water (4 mL), 10% aqueous sodium hydrogen carbonate solution (4 mL), 10% brine (4 mL), and water (4mL). After the organic layer was evaporated, toluene (4 mL) was added, and water was removed by azeotropic distillation. Toluene (4 mL) was added to the residue and this was used in the next step. HPLC analytical values for the toluene solution: 99.10% (toluene peak is disregarded).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375236B2
Source datasetuspto-grants-2008_05
ORD IDord-5c4e3441c1954cb5a0f09ab5a1d245bb
Source noteuspto-grants-2008_05