HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyloxyamine hydrochloride → O-Benzylhydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyloxyamine hydrochloride | HCID 102312 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | O-Benzylhydroxylamine | HCID 102313 | — |
Reaction Steps
O-Benzylhydroxylamine hydrochloride (1.71 g) was suspended in ethyl acetate, and the mixture was washed thoroughly with saturated aqueous sodium bicarbonate solution. the organic layer was dried (MgSO4), and evaporated under reduced pressure to leave O-benzylhydroxylamine as an oil. This was added dropwise to 3-trifluoromethylphenyl isocyanate (2.00 g), and the mixture was left to stand for 1 hour. The mixture was then dissolved in ethyl acetate and washed with 2M hydrochloric acid. The organic layer was separated, dried (MgSO4), and evaporated under reduced pressure to afford the product, yield 2.91 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856273 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-ae79c601ccf2447896dce61f8e26ea71 |
| Source note | uspto-grants-1999_01 |