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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833486Generated: October 30, 2026

Sodium Iodide → HCID 21317577, compound

https://huagongshe.com/reaction/1833486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant1-(p-Toluenesulfonyloxy)-4-acetoxy-5-(3-trifluoromethylphenoxy)pentaneHCID 21317629—
SolventAcetoneHCID 180—
ProductHCID 21317577HCID 21317577—

Reaction Steps

A solution of 1-(p-toluenesulfonyloxy)-4-acetoxy-5-(3-trifluoromethylphenoxy)pentane (125 g., 0.28 mole) and sodium iodide (126 g., 0.84 mole) in acetone (600 ml.) is allowed to stand at 25°-27° for 16 hours. The precipitated sodium tosylate is filtered off. Most of the acetone is evaporated from the filtrate and the residue is treated with 300 ml. of water. The oily product is taken up in ether, washed with dilute sodium thiosulfate solution, water, and brine, and dried over magnesium sulfate. The solvent is distilled in vacuo to yield 113 g. (97%) of the crude title compound as a yellowish oil which is used without further purification; pmr (CDCl3) 2.06 (3H, s CH3O); 3.20 (2H, t CH2I); 4.01 (2H, d CH2O); 5.20 (1H, m CHO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066675
Source datasetuspto-grants-1978_01
ORD IDord-f60af9af56724b8199dca98687a4cdee
Source noteuspto-grants-1978_01