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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732508Generated: October 31, 2026

1-Iodo-trans-1-octene-3-ol → 1-Iodo-3-(p-anisyldiphenylmethoxy)-trans-1-octene

https://huagongshe.com/reaction/1732508

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Iodo-trans-1-octene-3-olHCID 11043283—
Reactantp-Anisyldiphenylmethyl chlorideHCID 14836583—
SolventPyridineHCID 1049—
Product1-Iodo-3-(p-anisyldiphenylmethoxy)-trans-1-octeneHCID 20144623—

Reaction Steps

A mixture of 14.92 g. (0.0588 mole) of 1-iodo-trans-1-octene-3-ol (Example 74) and 18.2 g. (0.0588 mole) of p-anisyldiphenylmethyl chloride in 165 ml. of dry pyridine is heated at 60° C. for 18 hours under an inert atmosphere. The mixture is cooled and the solvent is evaporated in vacuo. The residue is partitioned between ether and water, and the organic phase is washed with water and saturated brine, dried (MgSO4), and evaporated. The residue is chromatographed upon 300 g. of Florisil® packed in hexane and the product is eluted with hexane and 4:1 hexane-benzene the yield a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237316
Source datasetuspto-grants-1980_12
ORD IDord-5ba596a955ce4b6291e552ca4bd61bd5
Source noteuspto-grants-1980_12