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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398788Generated: November 1, 2026

Hexane → [2-(4-Isopropoxy-butyloxy)-ethyl]-piperonyl-thioether

https://huagongshe.com/reaction/2398788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-4-(propan-2-yloxy)butaneHCID 21434041—
Reactant2-PiperonylthioethanolHCID 21434052—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DimethoxyethaneHCID 8071—
Product[2-(4-Isopropoxy-butyloxy)-ethyl]-piperonyl-thioetherHCID 21434047—

Reaction Steps

2.12 g (0.01 mol) of 2-piperonylthioethanol are added at room temperature over the course of 10 minutes, to a suspension of 0.48 g (0.01 mol) of 50% sodium hydride dispersion, which had been freed from the mineral oil with hexane, in 40 cc of 1,2-dimethoxy ethane. The mixture is stirred at 50° for 3 hours and a solution of 1.95 g (0.01 mol) of 1-bromo-4-isopropoxybutane in 30 cc of 1,2-dimethoxy ethane is subsequently added. The mixture is stirred at 60° over the course of 48 hours. After cooling to 20°, 100 cc of ether are added to the reaction mixture. The ether solution is extracted with saturated sodium chloride solution, dried over sodium sulphate and evaporated. The residue is purified by chromatography on silica gel with hexane/ethyl acetate (5:1), whereupon [2-(4-isopropoxy-butyloxy)-ethyl]-piperonylthioether is obtained as a slightly yellow, clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04025641
Source datasetuspto-grants-1977_05
ORD IDord-6dda5085ecb54457add35843f4d71386
Source noteuspto-grants-1977_05