HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254324Generated: October 26, 2026
Thiophene → 2-(7-Methoxycarbonyl-1-oxoheptyl)thiophene
https://huagongshe.com/reaction/2254324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Chloroacetic anhydride | HCID 10946 | — |
| Reactant | 8-Methoxy-8-oxooctanoic acid | HCID 554191 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 2-(7-Methoxycarbonyl-1-oxoheptyl)thiophene | HCID 19745238 | 91% |
Reaction Steps
In 50 ml of dichloroethane were dissolved 9.41 g (0.05 mole) of suberic acid monomethyl ester 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 60° C. for 5 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 11.5 g of 2-(7-methoxycarbonyl-1-oxoheptyl)thiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05235068 |
|---|
| Source dataset | uspto-grants-1993_08 |
|---|
| ORD ID | ord-3c9d73751140432cab76c4d321254801 |
|---|
| Source note | uspto-grants-1993_08 |
|---|