HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methane → 2-Hydroxy-4-dodecyloxy-4'-chlorobenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | 1-Bromododecane | HCID 8919 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (4-Chlorophenyl)(2,4-dihydroxyphenyl)methanone | HCID 519532 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | (+-)-2-Butanol | HCID 6568 | — |
| Product | 2-Hydroxy-4-dodecyloxy-4'-chlorobenzophenone | HCID 12084297 | 64.5% |
Reaction Steps
A mixture of 20 g (80 mmol) of 2,4-dihydroxy-4'-chlorobenzophenone, 21.9 g (88 mmol) of 1-bromododecane and 8.4 g (100 mmol) of sodium hydrogen carbonate in 77.6 g of sec-butyl alcohol and 25.6 g of H2O is heated with stirring and maintained at reflux for 20 h. The reaction mixture is stirred for an additional 15 min in the presence of 0.8 g of activated charcoal and is then filtered while hot. After the filtrate has cooled, the product crystallizes. It is recrystallized from sec-butyl alcohol to give 21.5 g of pale yellow crystals having a melting point of 61°-63° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05756793 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-4077fbbd5ffc4912b3743a37ddcfc6bb |
| Source note | uspto-grants-1998_05 |