HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → (3-Acetyloxy-5-carbonochloridoylphenyl) acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,5-Diacetoxybenzoic Acid | HCID 539869 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (3-Acetyloxy-5-carbonochloridoylphenyl) acetate | HCID 11368883 | 83% |
Reaction Steps
A stirring mixture of 68.2 g (0.29 mole) of 3,5-diacetoxybenzoic acid and 21 ml (0.29 mole) of thionyl chloride in 150 ml of dry benzene was heated in an oil bath at 80°-90° C. for 2 hours. After cooling the benzene was removed in vacuo to leave 3,5-diacetoxybenzoyl chloride as a tan, solid which was recrystallized from cyclohexane as colorless crystals, mp 87°-89° C., 61.8 g (83% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04036857 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-8d18185f9e78458cb24ec2c6cfdb123c |
| Source note | uspto-grants-1977_07 |