HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559070Generated: October 26, 2026
Sodium Carbonate → Ethyl 2-[4-(5-chlorothiophen-2-yl)-phenoxy]-4-cyclohex-1-enylbutanoate
https://huagongshe.com/reaction/559070
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Chlorothiophene-2-boronic acid | HCID 2734324 | — |
| Reactant | Ethyl 2-[(4-bromophenyl)oxy]-4-cyclohex-1-en-1-ylbutanoate | HCID 66999225 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 2-[4-(5-chlorothiophen-2-yl)-phenoxy]-4-cyclohex-1-enylbutanoate | HCID 66999601 | 73% |
Reaction Steps
0.18 g (0.04 equivalent) of Pd(PPh3)4 and then 1.2 g (0.0084 mol) of 5-chloro-2-thiopheneboronic acid are added to a solution of 1.4 g (0.0038 mol) of ethyl 2-[(4-bromophenyl)oxy]-4-cyclohex-1-en-1-ylbutanoate in 20 ml of dimethoxyethane. 4.2 ml of 2M sodium carbonate solution are added at room temperature. The reaction mixture is stirred overnight and then refluxed for 2 hours. After cooling to room temperature, the mixture is taken up in water and extracted with ethyl acetate. The extract is washed with 1N sodium hydroxide and then with saturated aqueous NaCl solution and finally dried over Na2SO4. After concentrating, the black oil obtained is purified by flash chromatography (95/5 heptane/ethyl acetate). 1.1 g of a thick oil are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08063067B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-9d41e5168a9843aea2dfe176500b558d |
|---|
| Source note | uspto-grants-2011_11 |
|---|