HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 3-(2-Amino-benzyl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 3-(Amino-benzoyl)thiophene | HCID 12750541 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | 3-(2-Amino-benzyl)thiophene | HCID 12750561 | — |
Reaction Steps
14.8 g of 3-(amino-benzoyl)thiophene, 23.8 g of solid potassium hydroxide and 19.6 g of hydrazine hydrate are heated to the boil at reflux in 180 cc of diethylene glycol for 3 hours. After diluting the reaction mixture with ice water, extraction is effected with ether. The ether phase is washed thrice with water, is dried with sodium sulphate and concentrated. 3-(2-amino-benzyl)thiophene is obtained in the form of a light yellow oil having a B.P. of 121°-123° 10.05 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03959282 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-65be94c783ec478c9d728355b674629b |
| Source note | uspto-grants-1976_05 |