HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybiphenyl → 4-Acetoxybiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Acetoxybiphenyl | HCID 346066 | 95.8% |
Reaction Steps
Into a 3-liter, 4-way flask equipped with a reflux cooling tube, 373.8 g of acetic anhydride and 248.0 g (1.46 mol) of 4-phenylphenol were introduced and the mixture was heated to cause reaction for 3 hours under agitation while keeping the temperature in the flask at 130° C. After the reaction, the reflux pipe was replaced with a distillation pipe and acetic anhydride and acetic acid were removed by distillation under decompression, after which n-heptane was added and the mixture was cooled. The precipitated crystal was filtered out and dried to obtain 296.8 g of 4-acetoxybiphenyl in a white crystal form. The yield relative to the material 4-phenylphenol was 96% (mol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08816135B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-b137eaf787404a10819219a758135071 |
| Source note | uspto-grants-2014_08 |