HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → O-[4-(tert-butyl-diphenyl-silanyloxy)-butyl]-hydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2-[4-(Tert-butyl-diphenyl-silanyloxy)-butoxy]-isoindole-1,3-dione | HCID 22286313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | O-[4-(tert-butyl-diphenyl-silanyloxy)-butyl]-hydroxylamine | HCID 22286549 | 90% |
Reaction Steps
A solution of 2-[4-(tert-butyl-diphenyl-silanyloxy)-butoxy]-isoindole-1,3-dione (11.1 g, 23.4 mmol) in dichloromethane (100 ml) was treated with methylhydrazine. The reaction mixture was stirred overnight and was filtered. The filtrate was concentrated and purified by column chromatography [hexane/ethyl acetate (3.5/1)] to afford O-[4-(tert-butyl-diphenyl-silanyloxy)-butyl]-hydroxylamine (7.2 g, 90% yield) as a colorless oil: 1H NMR (400 MHz, CDCl3) δ 7.62-7.66(4H, m), 7.33-7.42 (6H, m), 3.64-3.68(4H), 1.54-1.70 (4H, m), 1.02 (9H, s); MS (APCI+)=344.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07411001B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-58efa8e4e80d432fbb538fdd44eb53d8 |
| Source note | uspto-grants-2008_08 |