HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332872Generated: October 29, 2026
Sodium hydride → (E)-ethyl 3-(4-((6-methoxy-2-(4-methoxyphenyl)-1-oxidobenzo[b]thiophen-3-yl)oxy)phenyl)-2-methylacrylate
https://huagongshe.com/reaction/332872
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (E)-ethyl 3-(4-hydroxyphenyl)-2-methylacrylate | HCID 14920484 | — |
| Reactant | 3-Bromo-6-methoxy-2-(4-methoxyphenyl)benzothiophene 1-oxide | HCID 15959468 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-ethyl 3-(4-((6-methoxy-2-(4-methoxyphenyl)-1-oxidobenzo[b]thiophen-3-yl)oxy)phenyl)-2-methylacrylate | HCID 86730657 | 86% |
Reaction Steps
To a solution of (E)-ethyl 3-(4-hydroxyphenyl)-2-methylacrylate (92 mg, 0.445 mmol) in DMF (2.0 mL) was added sodium hydride (60% suspension in oil, 17.79 mg, 0.445 mmol), the resulting mixture was allowed to stir for 30 min at room temperature. To the solution was added 3-bromo-6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophene 1-oxide (125 mg, 0.342 mmol) as a suspension in DMF (2.0 mL). The reaction was heated to 80° C. for 15 h. Upon completion the reaction was cooled to room temperature, quenched with water and extracted with EtOAc. The combined organic layers were then washed with water, sat. aq. NaHCO3, brine and then collected (phase separator) and concentrated in vacuo to afford the crude product. The crude material was purified by column chromatography (SiO2, 0-70% EtOAc/Heptane) to afford (E)-ethyl 3-(4-((6-methoxy-2-(4-methoxyphenyl)-1-oxidobenzo[b]thiophen-3-yl)oxy)phenyl)-2-methylacrylate (144 mg, 0.294 mmol, 86% yield). LC/MS (m/z, MH+): 491.3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877801B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-d88c4e5bab434aa0bb673b95abdfd030 |
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| Source note | uspto-grants-2014_11 |
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