HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254335Generated: October 25, 2026
Thiophene → 2-(3,4,5-Trimethoxybenzoyl)thiophene
https://huagongshe.com/reaction/2254335
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | 3,4,5-Trimethoxybenzoic Acid | HCID 8357 | — |
| Reactant | Chloroacetic anhydride | HCID 10946 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 2-(3,4,5-Trimethoxybenzoyl)thiophene | HCID 19745233 | 41.5% |
Reaction Steps
In 50 ml of dichloroethane were dissolved 10.6 g (0.05 mole) of 3,4,5-trimethoxybenzoic acid and 9.83 g (0.0575 mole) of monochloroacetic anhydride. To the resulting solution were added 5.47 g (0.065 mole) of thiophene and 0.71 g of boron trifluoride-diethyl ether complex and the resulting mixture was then stirred at 65° 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 5.77 g of 2-(3,4,5-trimethoxybenzoyl)thiophene.
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-f732a69611604ab9a29d41118ece847c |
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| Source note | uspto-grants-1993_08 |
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