HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706344Generated: October 29, 2026
Hydrazine hydrate (1:1) → HCID 21708333, compound
https://huagongshe.com/reaction/706344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 89535922 | HCID 89535922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21708333 | HCID 21708333 | 79.9% |
Reaction Steps
To a stirred solution of (2-(thiazol-2-yl)phenyl)methanol (0.95 g, 5.1 mmol) in THF (15 mL) was added phthalimide (1.12 g, 7.65 mmol), triphenylphosphine (2.0 g, 7.65 mmol). The mixture was cooled in an ice-water bath and diisopropyl azodicarboxylate (3.1 g, 15.3 mmol) was added dropwise. After the addition, the mixture was stirred at 0° C. for 30 min, and at rt for 18 h. The mixture was then filtered and the filtrate was evaporated. The residue was purified by column chromatography to yield 2-(2-(thiazol-2-yl)benzyl)isoindoline-1,3-dione (1.1 g) as a white solid. To a stirred solution of 2-(2-(thiazol-2-yl)benzyl)isoindoline-1,3-dione (400 mg, 1.25 mmol) in ethanol (10 mL) was added dropwise hydrazine hydrate (160 mg, 3.1 mmol). The mixture was heated at 70° C. for 1 h. After cooling to rt, the mixture was filtered, and the filtrate was evaporated. The residue was purified by column chromatography to yield (2-(thiazol-2-yl)phenyl)methanamine (190 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09174984B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-5bfcb6851a884359b12e75d012ceb837 |
|---|
| Source note | uspto-grants-2015_11 |
|---|