Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Heptanoic Acid | HCID 8094 | — |
| Reactant | Chloroacetic anhydride | HCID 10946 | — |
| Reactant | 4-Acetoxybiphenyl | HCID 346066 | — |
| Solvent | 1,1,1,2-Tetrachloroethane | HCID 12418 | — |
| Product | HCID 19745245 | HCID 19745245 | 74% |
Reaction Steps
In 50 ml of tetrachloroethane were dissolved 6.51 g (0.05 mole) of heptanoic acid and 9.83 g (0.0575 mole) of monochloroacetic anhydride. To the resulting solution were added 12.74 g (0.06 mole) of 4-acetoxybiphenyl and 0.8 g of boron trifluoride-diethyl ether complex and the resulting mixture was then stirred at 100° C. for 10 hours. After completion of the reaction, the reaction solution was cooled and washed with 5% aqueous sodium carbonate solution and water in this order. The organic layer was concentrated under reduced pressure to obtain 12.0 g of 4-acetoxy-4'-heptanoylbiphenyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05235068 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-04cc24177625414d9b30bde1c937c684 |
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| Source note | uspto-grants-1993_08 |
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