HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 4-Phenylbutyric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | gamma-Phenyl-gamma-butyrolactone | HCID 13884 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Product | 4-Phenylbutyric Acid | HCID 4775 | — |
Reaction Steps
For example, a known compound, γ-phenyl-γ-butyrolactone having a melting point of 36° C. to 37° C. is reacted with a phenol derivative having the general formula: ##STR9## wherein R2 represents a hydrogen atom or an alkyl group having 1 to 3 carbon atoms in the presence of a base such as sodium alkoxide, potassium alkoxide, sodium hydroxide, potassium hydroxide, sodium hydride, or sodium metal to form a 4-phenyl butyric acid derivative having the general formula: ##STR10## wherein R2 is the same as defined above,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04766116 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-42d700edab324b409ac43f27231f3fb1 |
| Source note | uspto-grants-1988_08 |