HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-Iodobenzo[d][1,3]dioxol-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(6-Iodo-2H-1,3-benzodioxol-5-yl)acetamide | HCID 53488067 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Iodobenzo[d][1,3]dioxol-5-amine | HCID 53488068 | 98.5% |
Reaction Steps
A solution of N-(6-iodobenzo[d][1,3]dioxol-5-yl)acetamide (200 mg, 0.656 mmol) and NaOH (1.31 g, 32.8 mmol) in ethanol (26 mL) and water (6 mL) was heated to reflux with stirring for 4 h. The mixture was cooled and the solvent was removed under vacuum. The residue was partitioned between methylene chloride (100 mL) and water (100 mL). The organic layer was washed with water (2×100 mL), dried (MgSO4) and evaporated under vacuum to give 6-iodobenzo[d][1,3]dioxol-5-amine (170 mg, 98%) as orange solid. LCMS: 264 [M+1]+; 1H NMR (DMSO-d6) δ 4.88 (s, 2H), 5.87 (s, 2H), 6.47 (s, 1H), 7.07 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09402832B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-8b74519ed7674fdcb4087268b86d389e |
| Source note | uspto-grants-2016_08 |