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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439118Generated: November 2, 2026

2,6-Lutidine → 1-Chloro-3-triphenylmethoxyhexane

https://huagongshe.com/reaction/1439118

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantChlorobenzeneHCID 7964—
ReactantBromotriphenylmethaneHCID 11692—
Reactant1-Chlorohexan-3-olHCID 18921007—
SolventWaterHCID 962—
Product1-Chloro-3-triphenylmethoxyhexaneHCID 20381013—

Reaction Steps

A stirred solution of 27.3 g. (0.20 moles) of 1-chloro-3-hexanol, 77.6 g. (0.24 moles) of triphenylmethyl bromide, 30.0 g. (0.28 moles of 2,6-lutidine, and 200 ml. of chlorobenzene is heated at 95° C. for 1 hour. The cooled mixture is treated with water, and the organic phase is washed successively with water and saturated sodium chloride solution. The solution is dried over magnesium sulfate and concentrated. Column chromatography of the residue on Florisil affords the subject compound as an oil, λ max. 1600, 1030, and 705 cm-1 (triphenylmethoxy group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE029469
Source datasetuspto-grants-1977_11
ORD IDord-b47f0a40932343bda4a142acad0d6142
Source noteuspto-grants-1977_11