HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Methyl 5-(p-benzyloxyphenyloxy)-2,2-dimethylpentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-(p-Benzyloxyphenoxy)-2,2-dimethylpentanoic acid | HCID 13422046 | — |
| Product | Methyl 5-(p-benzyloxyphenyloxy)-2,2-dimethylpentanoate | HCID 23042682 | — |
Reaction Steps
In 100 ml of tetrahydrofuran was dissolved 9 g of 5-(p-benzyloxyphenoxy)-2,2-dimethylpentanoic acid. The resulting solution was treated with a diazomethane-ether solution in a conventional manner to give methyl 5-(p-benzyloxyphenyloxy)-2,2-dimethylpentanoate. The thus obtained ester was dissolved in 200 ml of methanol and 10% palladium-carbon was added to the solution. The mixture was reacted with stirring in a hydrogen atmosphere under normal pressure until a theoretical amount of hydrogen was absorbed. Palladium-carbon was removed by filtration and the solvent was removed by distillation under reduced pressure to give the desired product, methyl 5-(p-hydroxyphenoxy)-2,2-dimethylpentanoate as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04794113 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-59cabcc041e243ffa7562e8c8ae523bc |
| Source note | uspto-grants-1988_12 |