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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050687Generated: October 27, 2026

N,N,N',N'-Tetramethylethylenediamine → Tributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannane

https://huagongshe.com/reaction/1050687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantHexaneHCID 8058—
ReactantTributyltin ChlorideHCID 15096—
Reactant3,4-EthylenedioxythiopheneHCID 4421864—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductTributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannaneHCID 1589105340%

Reaction Conditions

Temperature35 °C

Reaction Steps

1.5M n-BuLi in hexane (53 mL, 80 mmol) was added in small portions to a solution of 2,3-dihydrothieno[3,4-b][1,4]dioxine (10.00 g, 80 mmol) and tetramethylethylenediamine (12.0 mL, 80 mmol) in tetrahydrofuran (100 mL) stirred under argon and cooled in a dry ice/acetone bath. The reaction mixture was heated to 35° C., stirred at this temperature for 1 hour, and then cooled in a dry ice/acetone bath. Tributylstannyl chloride (20.3 mL), 75 mmol was then added, the mixture was allowed to warm up, and it was left at room temperature for 16 hours. The volatiles were removed under reduced pressure. The residue was diluted with toluene (100 mL) and chromatographed using a column filled with silica gel (500 mL) washed with 2% triethylamine in hexane (500 mL) to give tributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannane (12.17 g, 40%) of high purity. 1H NMR (400 MHz, CDCl3): δ 6.57 (s, 1H, thiophene), 4.15 (m, 4H, OCH2CH2O), 1.53 (m, 6H, Bu), 1.32 (quintet, J=7.3 Hz, 6H, Bu), 1.09 (m, 6H, Bu), 0.88 (t, J=7.3 Hz, 9H, Bu).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382424B2
Source datasetuspto-grants-2016_07
ORD IDord-f5fb9b8fb0b74fe6b8792a922b2cd76d
Source noteuspto-grants-2016_07