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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579736Generated: October 27, 2026

Hydrogen Peroxide → HCID 20136519, compound

https://huagongshe.com/reaction/579736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
ReactantBorane, tris(1-methylpropyl)-HCID 102559—
Reactant2,3-Bis(4-methoxyphenyl)thiopheneHCID 11403717—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 20136519HCID 2013651941%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04749712
Source datasetuspto-grants-1988_06
ORD IDord-16db53b36520447ab9bd579916159426
Source noteuspto-grants-1988_06