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 the product of Example 13, Step A, 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 2 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 | US06770778B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-47f0e6af8a0c45edb9aa41879ae2d214 |
| Source note | uspto-grants-2004_08 |