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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395370Generated: October 29, 2026

Thionyl Chloride → HCID 12882333, compound

https://huagongshe.com/reaction/1395370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-Phenoxybenzyl alcoholHCID 26295—
ReactantHCID 13097323HCID 13097323—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
ProductHCID 12882333HCID 1288233334.8%

Reaction Steps

Pyridine (1.68 g) and thionyl chloride (2.5 g) are added to a mixture of 3'-chloro-3,3-dimethyl-spiro[cyclopropane-1,1'-indene]-2-carboxylic acid (5.0 g; 0.02 mole) and ether (50 ml). After two hours at room temperature, pyridine (1.68 g) and m-phenoxybenzyl alcohol (4.0 g) are added and the reaction mixture stirred at room temperature overnight. The reaction mixture is then washed with water, the ether fraction dried over magnesium sulfate and evaporated to dryness. The residue is purified on a dry column (silica gel; 20% methylene chloride:hexane) to afford 3.0 g of title compound, a yellow-orange liquid. The sample is 90-95% pure by NMR, and shows an ester carbonyl stretch at 1730 cm-1 in IR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04203918
Source datasetuspto-grants-1980_05
ORD IDord-fc3f92d7dded4d2b9e5d4ef3cdcdabd2
Source noteuspto-grants-1980_05