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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732249Generated: November 4, 2026

Sulfuric Acid → 1H-Isoindol-3-amine, 5,6-diethoxy-4-fluoro-, sulfate (1:1)

https://huagongshe.com/reaction/732249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTriethylamineHCID 8471—
Reactant4,5-Diethoxy-3-fluorophthalonitrileHCID 22929841—
CatalystHCID 178502593HCID 178502593—
Solvent1,2-DimethoxyethaneHCID 8071—
Product1H-Isoindol-3-amine, 5,6-diethoxy-4-fluoro-, sulfate (1:1)HCID 1158805472%

Reaction Conditions

Temperature-23 °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 −23° C. under hydrogen atmosphere (atmospheric pressure) for 29 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. To one of them, triethylamine (0.14 mL, 1 mol) was added, and the mixture was stirred at 60° C. for three hours and concentrated at 40° C. under reduced pressure. Methanol (2.3 mL) and 1,2-dimethoxyethane (6.9 mL) were added to the residue, then sulfuric acid (0.11 mL, 2 mol) was added on ice, and the mixture was stirred. Precipitated crystals were filtered, washed with a 5% methanol-1,2-dimethoxyethane solution, and dried at room temperature under reduced pressure to give 0.45 g of the title compound (yield: 72%) as grayish white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585982B2
Source datasetuspto-grants-2009_09
ORD IDord-71d5a13e2cff468781edfaff52249ccd
Source noteuspto-grants-2009_09