HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → O-(2,2-dimethyl-1,3-dioxan-5-yl)Hydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2-(2,2-Dimethyl-[1,3]dioxan-5-yloxy)-isoindole-1,3-dione | HCID 22025675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | O-(2,2-dimethyl-1,3-dioxan-5-yl)Hydroxylamine | HCID 22025693 | 106.3% |
Reaction Steps
To a stirring solution of 2-(2,2-dimethyl-[1,3]dioxan-5-yloxy)-isoindole-1,3-dione (1.72 g, 6.20 mmol) in dichloromethane (15 mL) at 0° C. under nitrogen was added methylhydrazine (0.36 mL, 6.82 mmol) and allowed to warm to room temperature. After stirring for two hours the reaction mixture was concentrated in vacuo and charged with diethylether. The solids were filtered off and the filtrate was collected and concentrated to afford O-(2,2-dimethyl-[1,3]dioxan-5-yl)-hydroxylamine as a yellow oil (0.97 g, 100%). 1H NMR (400 MHz; DMSO-d6) δ 5.98 (bs, 2H), 3.84-3.87 (m, 2H), 3.66-3.68 (m, 2H), 3.30-3.35 (m, 1H), 1.29 (s, 3H), 1.22 (s, 3H); MS (APCI+)=147.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06960614B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-905d5ab4f37c4c6391660544dab19f64 |
| Source note | uspto-grants-2005_11 |