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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980516Generated: October 31, 2026

Methyl iodide → HCID 20401742, compound

https://huagongshe.com/reaction/1980516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 13392351HCID 13392351—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 20401742HCID 2040174279.2%

Reaction Steps

A solution of 4.0 g (15.3 mmol) of (1,1'-biphenyl-4-yl)chloromethyldimethylsilane in 20 ml of tetrahydrofuran was cooled to -78°, and 12.5 ml (16.8 mmol) of 1.35 molar sec-butyllithium in hexane was slowly dripped in followed by addition of 2.42 ml (16.1 mmol) of tetramethylethylenediamine. After stirring for one hour at -78°, the solution was warmed to -55° and 1.43 ml (22.9 mmol) of methyl iodide in 5 ml of tetrahydrofuran was added dropwise. The mixture was stirred another 30 minutes at -50°, warmed to room temperature, poured into saturated aqueous ammonium chloride, and extracted with ether. The ether extracts were washed with water and brine, dried over magnesium sulfate, and evaporated to give 3.33 g (65%) of the title compound contaminated by about 18% of an impurity: nmr (CDCl3) 0.3 (s, 2.7H, impurity), 0.4 (6H, s), 1.5 (3H, d, J=7 Hz), 3.5 (1H, q, J=7 Hz) and 7.3-7.7 (m, 13H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04510136
Source datasetuspto-grants-1985_04
ORD IDord-7f16e595b5374471ab13567d7832ac11
Source noteuspto-grants-1985_04