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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | 4,5-Diethoxy-3-fluorophthalonitrile | HCID 22929841 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 6-Aminomethyl-3,4-diethoxy-2-fluorobenzonitrile sulfate | HCID 86623001 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07585982B2 |
|---|
| Source dataset | uspto-grants-2009_09 |
|---|
| ORD ID | ord-2f06102da0fb45d8831890ff6feb0c55 |
|---|
| Source note | uspto-grants-2009_09 |
|---|