HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydroxylamine → HCID 13137243, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydroxylamine | HCID 11647 | — |
| Reactant | 4-Hydroxy-4-methyl-5-(prop-2-en-1-yl)cyclopent-2-en-1-one | HCID 12879872 | — |
| Product | HCID 13137243 | HCID 13137243 | 91.2% |
Reaction Steps
2-Allyl-3-hydroxy-3-methyl-4-cyclopentenone (15.2 g) was dropwise added to a 25% aqueous solution of N-methylhydroxylamine (30 g) in the same flask as used in Example 1 at a temperature of 15° to 25° C. for 1 hour. At the same temperature, the reaction mixture was kept for 2 hours. After completion of the reaction, the mixture was treated and purified in the same manner as in Example 5 to obtain 2-allyl-3-methyl-4-(N-hydroxy-N-methylamino)-2-cyclopentenone (16.5 g). Yield, 91%. nD20 1.5102.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04665174 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-a312931716ed4861805bf34c5dd0be10 |
| Source note | uspto-grants-1987_05 |