HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → 4-Methoxy-benzo[b]thiophen-3-yl-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Ethyl 4-[(3-methoxyphenyl)sulfanyl]-3-oxobutanoate | HCID 21816283 | — |
| Product | 4-Methoxy-benzo[b]thiophen-3-yl-acetic acid ethyl ester | HCID 21816272 | 59% |
Reaction Steps
4-(3-methoxy-phenylsulfanyl)-3-oxo-butyric acid ethyl ester (10.9 g, 40.62 mmol) is added to methanesulfonic acid (26.6 mL, 406 mmol). The mixture is stirred at room temperature for 30 minutes. The reaction mixture is poured into ice-water (300 g) and extracted with EtOAc (100 mL×2). The combined organic layers are dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product is purified by flash chromatography eluting with 20% EtOAc/Hexanes. The appropriate fractions are combined and concentrated under reduced pressure to afford the title compound (6.00 g, 59%). ES/MS n/e 251.0 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863302B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-a18fbf41db104f23a8d6e5401c2f5d4d |
| Source note | uspto-grants-2011_01 |