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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166441Generated: October 30, 2026

Pyridine → 3-Octadecyloxycarbonyloxy-1-[6-(triphenylmethoxy)hexyloxyl]-2-methylenepropane

https://huagongshe.com/reaction/2166441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
ReactantCarbonochloridic acid, octadecyl esterHCID 103922—
Reactant3-[6-(Triphenylmethoxy)hexyloxy]-2-methylenepropan-1-olHCID 23039633—
SolventDichloromethaneHCID 6344—
Product3-Octadecyloxycarbonyloxy-1-[6-(triphenylmethoxy)hexyloxyl]-2-methylenepropaneHCID 23039640—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 3-[6-(triphenylmethoxy)hexyloxy]-2-metylenepropane-1-ol (from Preparation 46) (1.5 g) and pyridine (4.5 ml) in methylene chloride (15 ml) was cooled in an ice/water bath and octadecyloxycarbonyl chloride (1.3 g) was added. After stirring for 10 minutes at 0° C. the temperature was raised to 22° C. for 5 hours. Ether (15 ml) was added, and the mixture was filtered. The filtrate was evaporated to dryness in vacuo, and the residue was purified through a column of silica gel 60 (70-230 mesh, 15 g) eluting with ether/methylene chloride 1:1. Further purification was achieved by chromatography on Waters PrepLC®/System 500A using a prepPAK®-500/SILICA cartridge with ether/methylene chloride/pentane 1:1:3 as eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945098
Source datasetuspto-grants-1990_07
ORD IDord-b9b334019e1a4640b0a3ac8ad7ba8dc2
Source noteuspto-grants-1990_07