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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483876Generated: October 31, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 59791330, compound

https://huagongshe.com/reaction/1483876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1-Chloro-3-iodopropaneHCID 81363—
Reactanttert-Butyl[(furan-2-yl)methoxy]dimethylsilaneHCID 10976930—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventEthylacetate heptaneHCID 21899848—
ProductHCID 59791330HCID 5979133075%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-(t-butyldimethylsilyloxymethyl)furan (5 g, 0.023 mol) in THF (48 mL) was dried over 3 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416353B2
Source datasetuspto-grants-2016_08
ORD IDord-b910b28cfaae4363a9df48e21ca04bcb
Source noteuspto-grants-2016_08