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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918008Generated: October 31, 2026

HCID 54512866, compound → HCID 54521914, compound

https://huagongshe.com/reaction/918008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54512866HCID 54512866—
ReactantHCID 86732997HCID 86732997—
SolventBenzeneHCID 241—
ProductHCID 54521914HCID 54521914—

Reaction Steps

A solution of 4.3 g (0.015 mol) of 5-(4-bromo-3-methyl-2-butenyloxy)-1,3-benzodioxol in 50 cc of benzene is added at 25° to 1.7 g (0.015 mol) of sodium-isobutylthio alcoholate in 30 cc of benzene. The mixture is kept at reflux temperature for 13 hours, is subsequently filtered, washed with saturated salt solution and evaporated. The remaining yellow oil is chromatographed with hexane/ethyl acetate 7:1 on silica gel, whereby colourless 5-(4-isobutylthio-3-methyl-2-butenyloxy)-1,3-benzodioxol is obtained. nD20 = 1.5463.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03968235
Source datasetuspto-grants-1976_07
ORD IDord-040c70935eeb41af9a7438f389e9d46e
Source noteuspto-grants-1976_07