Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605792Generated: October 31, 2026

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

https://huagongshe.com/reaction/1605792

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 numberUS03950406
Source datasetuspto-grants-1976_04
ORD IDord-27c904114d49409889ed77e95215033e
Source noteuspto-grants-1976_04