HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → O-(tert-Butyldiphenylsilyl)hydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | O-(tert-Butyldiphenylsilyl)hydroxylamine | HCID 11737343 | — |
Reaction Steps
Hydroxylamine hydrochloride (3.48 g) and triethylamine (7 ml) were stirred for 0.25 hours in DMF (50 ml) at 0° C. tert-Butyldiphenylsilyl chloride (13 ml) was added and the mixture was stirred for 1 hour. The mixture was partitioned between pentane (500 ml) and water (100 ml), the layers separated and the aqueous phase extracted with ethyl acetate (2×100 ml). The organic layers were combined, washed with brine (50 ml), dried over magnesium sulphate and the solvent was removed in vacuo. The crude product was triturated with pentane (20 ml) yielding the pure title compound as white solid (4.04 g), m.p.t. 85°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04684641 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-87387689be1e4fb4aa903dde6aeb2236 |
| Source note | uspto-grants-1987_08 |