HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Acetyl-6-(bromomethyl)-4-hydroxy-2H-pyran-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Acetyl-4-hydroxy-6-methyl-2H-pyran-2-one | HCID 54678494 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Acetyl-6-(bromomethyl)-4-hydroxy-2H-pyran-2-one | HCID 54723916 | 47% |
Reaction Steps
A mixture of 3-acetyl-4-hydroxy-6-methylpyran-2-one (52 parts), N-bromosuccinimide (54 parts) and dichloromethane (1060 parts) were stirred at 20°-25° C. for about 4-5 hours under exposure to UV light. The dichloromethane solution was washed with water (2×500 cm3) to remove the succinimide, dried over magnesium sulphate, filtered and the solvent removed at 40° C./20 mm to leave 3-acetyl-6-bromomethyl-4-hydroxypyran-2-one (70 parts, 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05443970 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-7940590eee534e9bb31d2a8fb743e35c |
| Source note | uspto-grants-1995_08 |