HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → HCID 21293763, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21293762 | HCID 21293762 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21293763 | HCID 21293763 | — |
Reaction Steps
N-acetoxy-N-(1-dibenzofur-3-ylethyl) acetamide. Acetic anhydride (9.0 mL) was added to a solution of the crude hydroxylamine, prepared as in step c, and triethyl amine (12.4 mL) in methylene chloride (50 mL). The reaction was stirred overnight, then washed with cold water and 3 N HCl. The methylene chloride layer was dried (Na2SO4) and concentrated to give a yellowish oil. This residue was chromatographed on 100 g of silica gel, eluting with 20% ethyl acetate in hexanes to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04822811 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-adea5f33ead14d32a4f1d376c0b19330 |
| Source note | uspto-grants-1989_04 |