Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Veratrole | HCID 7043 | — |
| Reactant | Chloroacetic anhydride | HCID 10946 | — |
| Reactant | 1-Cyclohexene-1-carboxylic acid | HCID 69470 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 12238904 | HCID 12238904 | 59% |
Reaction Steps
In 50 ml of dichloroethane were dissolved 6.31 g (0.05 mole) of 1-cyclohexene-1-carboxylic acid and 10.26 g (0.06 mole) of monochloroacetic anhydride. To the resulting solution were added 8.98 g (0.065 mole) of 1,2-dimethoxybenzene and 0.71 g of boron trifluoridediethyl ether complex and the resulting mixture was then stirred at 75° C. for 6 hours. After completion of the reaction, the reaction solution was cooled and washed successively with water, 5% aqueous sodium carbonate solution and water. The organic layer was dried over, anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain 7.27 g of 4-(1-cyclohexenoyl)-1,2-dimethoxybenzene.
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-e4a777fb3fc545cfb787a2ffc68ecb86 |
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| Source note | uspto-grants-1993_08 |
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