HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 5-Bromo-2-[(3-iodo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yloxy)acetyl]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-1-(5-bromothiophen-2-yl)ethan-1-one | HCID 1988398 | — |
| Reactant | 3-Iodo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ol | HCID 10711463 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 5-Bromo-2-[(3-iodo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yloxy)acetyl]thiophene | HCID 70195143 | — |
Reaction Steps
A solution of 3-iodo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ol (4 g, 12.1 mmol), 2-bromoacetyl-5-bromothiophene (3.44 g, 12.1 mmol) and potassium carbonate (1.8 g, 13.3 mmol) in methyl ethyl ketone (100 ml), was heated under reflux for 3 h. The reaction medium was filtered and then concentrated in a rotary evaporator, and water and ethyl ether were added. After stirring and decantation, the organic phase was washed twice with water, dried over magnesium sulfate and concentrated in a rotary evaporator under vacuum at 40° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05905088 |
| Source dataset | uspto-grants-1999_05 |
| ORD ID | ord-5f19d11b409247419627fa73c80882d7 |
| Source note | uspto-grants-1999_05 |