HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetate → HCID 86735853, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetate | HCID 175 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Tert-Butylbenzenethiol | HCID 75454 | — |
| Reactant | Carbonochloridate | HCID 21226386 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | HCID 86735853 | HCID 86735853 | — |
Reaction Steps
This compound was prepared in the same manner as the 4-phenoxy derivative described in Example XXIX except p-t-butylthiophenol was added instead of phenol to the methanolic solution of KOH before the chloro compound was added in step C. The acetate was saponified to the alcohol by the addition of excess base to the methanol after the reaction of the chloro compound and the p-t-butylthiophenol was complete. The alcohol was then converted to the chloroformate by adding a pentane solution of the alcohol and pyridine to a pentane solution of phosgene as in step D of Example XXIX. The infrared spectrum confirmed that the alcohol was converted to the chloroformate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101522 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-8b13ca1dd39545948405a4218acbc83a |
| Source note | uspto-grants-1978_07 |