HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402219Generated: October 30, 2026
N,N,N',N'-Tetramethylethylenediamine → HCID 59791330, compound
https://huagongshe.com/reaction/402219
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | 1-Chloro-3-iodopropane | HCID 81363 | — |
| Reactant | tert-Butyl[(furan-2-yl)methoxy]dimethylsilane | HCID 10976930 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethylacetate heptane | HCID 21899848 | — |
| Product | HCID 59791330 | HCID 59791330 | 75% |
Reaction Steps
A solution of 2-(t-butyldimethylsilyloxymethyl)furan (5 g, 0.023 mol) in THF (48 mL) was dried over 3 {acute over (Å)} molecular sieves. After the sieves were removed, an additional 10 mL THF was added along with TMEDA (3.47 mL, 0.023 mol), and the solution was cooled to 0° C. in an ice bath. A solution of BuLi (10.1 mL of 2.5M in hexane, 0.025 mol) was added dropwise over 25 minutes. The mixture was allowed to stir for 1 hour. 1-chloro-3-iodopropane (5.64 g, 0.028 mol) was injected rapidly. After 2 hours TLC indicated completion. The solvent was evaporated, and the material was partitioned between ether (100 mL) and 5% citric acid (100 mL). The ether layer was washed with water (50 mL) and then brine (50 mL). The ether solution was dried with sodium sulfate, filtered, and evaporated. The resulting material was flashed on silica using 20/1 heptane/EtOAc. Appropriate fraction were combined and evaporated to yield 4.9 g (75% yield). TLC: Rf 0.6 (Heptane/EtOAc 5/1) 1H NMR: (CDCl3) δ 0.00 (s, 6H), 0.83 (s, 9H), 2.01 (p, 2H), 2.71 (t, 2H), 3.48 (t, 2H), 4.51 (s, 2H), 5.88 (d, 1H), 6.04 (d, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742086B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-13d3954f675e4108b8c47ab0161f58b2 |
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| Source note | uspto-grants-2014_06 |
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