HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Methyl 2-(3-methoxy-phenyl)-7-benzofuranacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(3-Methoxy-phenyl)-7-benzofurancarbaldehye | HCID 14995682 | — |
| Reactant | HCID 178505373 | HCID 178505373 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-(3-methoxy-phenyl)-7-benzofuranacetate | HCID 67875966 | — |
Reaction Steps
A mixture of 7.4 g of the product of Step A, 4.4 g of methyl methylsulfinyl methyl sulfide, 75 ml of tetrahydrofuran and 7 ml of Triton B was refluxed for one hour and then was poured into water and extracted with dichloromethane. The extracts were dried and concentrated to obtain 10 ml of produce which was dissolved in a 2N hydrochloric acid solution in methanol. The solution was stirred for 24 hours, treated with sodium bicarbonate, and stirred for one hour. After separating, extraction was carried out with ether and the extracts were washed and concentrated to obtain 9 g of product which was chromatographed on silica to obtain (eluant: hexane-ethyl acetate (9-1)) 4.3 g of the desired product which was used as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05182295 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-576f0007ad29438ab02c83b87e8a3219 |
| Source note | uspto-grants-1993_01 |