Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224560Generated: October 29, 2026

Iodine → HCID 20442063, compound

https://huagongshe.com/reaction/224560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 20442099HCID 20442099—
SolventDiethyl EtherHCID 3283—
ProductHCID 20442063HCID 20442063—

Reaction Steps

To a solution of E-1-tri-n-butystannyl-4-triethylsilyloxy-1-octene (11 g) in 200 ml ether is added 0.9 equivalents of iodine in one portion. After 25 minutes the color of the iodine has disappeared. An additional 0.1 equivalents of iodine is added in portions until the iodine color persists. The ether is removed in vacuo to provide (E)-1-iodo-4-triethylsilyloxy-1-octene. This residue is placed on a silica-gel column (240 g SilicAR CC-7) packed in hexane. A liter fraction of hexane contains 7.5 g of mostly tri-n-butyliodostannane. A 500 ml elution of benzene gives only a small amount of material. An elution with 600 ml of ether provides 7.0 g of 1-iodo-4-hydroxy-1-octene as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233231
Source datasetuspto-grants-1980_11
ORD IDord-77e362c3e6174ec4ad68607732740c78
Source noteuspto-grants-1980_11