HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 3-Iodobenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 3-Iodobenzylamine hydrochloride | HCID 2723861 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Iodobenzylamine | HCID 97012 | 94% |
Reaction Steps
To a stirred solution of 3-iodobenzylamine hydrochloride dissolved in distilled water (13.2 mL per gram) is added dropwise an aqueous ammonium hydroxide (5.3 mL per gram) solution. A yellow oil separates and is extracted into ethyl acetate (3×6.6 mL per gram). The ethyl acetate layer is dried over anhydrous sodium sulfate and evaporated on a rotovap to obtain 3-iodobenzylamine as a yellow oil (94% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05565185 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-5a6da5b638cd41c5b5f087ba6e736f13 |
| Source note | uspto-grants-1996_10 |