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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732251Generated: October 31, 2026

Sulfuric Acid → 6-Aminomethyl-3,4-diethoxy-2-fluorobenzonitrile sulfate

https://huagongshe.com/reaction/732251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant1,2-DimethoxyethaneHCID 8071—
Reactant4,5-Diethoxy-3-fluorophthalonitrileHCID 22929841—
CatalystHCID 178502593HCID 178502593—
SolventTriethylamineHCID 8471—
Product6-Aminomethyl-3,4-diethoxy-2-fluorobenzonitrile sulfateHCID 8662300176%

Reaction Conditions

Temperature-22 °C

Reaction Steps

A mixture of 4,5-diethoxy-3-fluorophthalonitrile (2.34 g, 10 mol) prepared in Preparation Example 1, sulfuric acid (0.56 mL, 10 mol), 20% palladium hydroxide-carbon (0.59 g, 50% hydrate) (20% palladium-carbon powder, palladium hydroxide type (hydrate), N.E. Chemical Corporation) and 1,2-dimethoxyethane (23 mL) was stirred at −22° C. under hydrogen atmosphere (atmospheric pressure) for 24 hours. After insoluble matter in the reaction mixture was filtered off, the residue was washed with methanol (23 mL) and the combined filtrate was divided into five equal portions. After one of them was concentrated at room temperature under reduced pressure, 1,2-dimethoxyethane (9.2 mL) was added thereto, and the mixture was stirred. Then, triethylamine (0.56 mL, 4 mol) was added dropwise thereto and the mixture was stirred at room temperature for one hour. Precipitated crystals were filtered, washed with a 5% methanol-1,2-dimethoxyethane solution, and dried at room temperature under reduced pressure to give 0.59 g of the ½ triethylamine solvate of the title compound (yield: 76%) as dark white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585982B2
Source datasetuspto-grants-2009_09
ORD IDord-2f06102da0fb45d8831890ff6feb0c55
Source noteuspto-grants-2009_09