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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 3,4-Ethylenedioxythiophene | HCID 4421864 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tributyl(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)stannane | HCID 15891053 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382424B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-f5fb9b8fb0b74fe6b8792a922b2cd76d |
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| Source note | uspto-grants-2016_07 |
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