HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579736Generated: October 27, 2026
Hydrogen Peroxide → HCID 20136519, compound
https://huagongshe.com/reaction/579736
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Borane, tris(1-methylpropyl)- | HCID 102559 | — |
| Reactant | 2,3-Bis(4-methoxyphenyl)thiophene | HCID 11403717 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20136519 | HCID 20136519 | 41% |
Reaction Steps
A solution of 2,3-bis(4-methoxyphenyl)thiophene (5.92 g, 20 mmole) in toluene (40 ml)/diethyl ether (130 ml) was treated with 1.6M n-butyl lithium (14 ml, 1.1 equiv.) and heated at reflux for 1.5 hours. The reaction mixture was cooled to -76° and treated dropwise with 1M tri-s-butylboron (22 ml, 1.1 equiv.). After 0.5 hours at -76°, the reaction mixture was stirred at 0° for 0.5 hours, recooled to -76° and treated with bromine (1 ml, 20 mmole) in 20 ml diethyl ether. The mixture was allowed to warm to room temperature, and then after 2 hours was treated sequentially with 50% (w/w) sodium hydroxide (2.3 ml) and 30% hydrogen peroxide (8 ml). The mixture was stirred overnight, and then extracted with ethyl acetate. The organic extracts were washed with water and brine, dried and concentrated in vacuo. Chromatography on a Waters Prep 500 (hexane/ethyl acetate, 9:1) provided the title compound (2.9 g, 41%) as an oil. Proton NMR was consistent with the assigned structure. Mass Spec. (MS): m/z 352 (M+), 323 (M--C2H5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04749712 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-16db53b36520447ab9bd579916159426 |
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| Source note | uspto-grants-1988_06 |
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