HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Allylhydroxylamine → HCID 178460156, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Allylhydroxylamine | HCID 420841 | — |
| Reactant | HCID 20291508 | HCID 20291508 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178460156 | HCID 178460156 | 95% |
Reaction Steps
2.6 g of 2- butyryl-5-(2-methylthioethyl)-cyclohexane-1,3-dione was allowed to react with 0.8 g of allyloxyamine at room temperature for 10 hours in 20 ml of ethanol. After completion of the reaction, the resulting reaction solution was treated as in Example 1 to obtain 3 g of the desired compound as colorless oily material. nD27 1.5402
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04249937 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-1d353722137c4772baa4bc6dd15dbb44 |
| Source note | uspto-grants-1981_02 |