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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461272Generated: October 29, 2026

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

https://huagongshe.com/reaction/461272

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, ν max. 1600, 1030, and 705 cm-1 (triphenylmethoxy group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04061672
Source datasetuspto-grants-1977_12
ORD IDord-51b14a3083bb48db93c36097f9292ae6
Source noteuspto-grants-1977_12