HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (2-Fluoro-4-nitrophenyl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-(2-Fluoro-4-nitrobenzyl)isoindoline-1,3-dione | HCID 70847669 | — |
| Product | (2-Fluoro-4-nitrophenyl)methanamine | HCID 45121148 | 41.5% |
Reaction Steps
To a solution of 2-(2-fluoro-4-nitrobenzyl)isoindoline-1,3-dione (1.35 g, 4.48 mmol) in tetrahydrofurane 65% hydrazine monohydrate (1.3 mL, 4 eq) was added. The mixture was refluxed for 6 h. After the starting material was consumed, the mixture was cooled down to room temperature and treated with potassium bicarbonate to pH 12˜13. Then it was extracted with ethyl acetate and washed with brine. Drying over magnesium sulfate, evaporation of the ethyl acetate and purification by column chromatography gave (2-fluoro-4-nitrophenyl)methanamine (316 mg, 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08937092B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-6743afb4006145d99b249d262d228b6e |
| Source note | uspto-grants-2015_01 |