HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 4-methoxyphenyl ketone → 2-Hydroxy-1-(4-methoxyphenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxy-1-(4-methoxyphenyl)ethanone | HCID 77786 | — |
Reaction Steps
It is used in the synthesis of MOPMN, above, and was synthesized from 2-bromo-4'-methoxyacetophenone (Aldrich). The 2-bromo-4'-methoxyacetophenone was refluxed in 20% water and N-methyl-2-pyrrolidinone for 10 hours at 105° C. The product was extracted with ethylether, dried over MgSO4, the ether evaporated and the dry solid recrystallized before use. Melting point 98.5°-100.5° C. and the NMR corresponds to the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05314815 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-ebc5830933c54250a851bf8a2fd0df97 |
| Source note | uspto-grants-1994_05 |