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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420419Generated: November 3, 2026

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

https://huagongshe.com/reaction/2420419

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-octen-3-ol (Example 955) 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 numberUS04110368
Source datasetuspto-grants-1978_08
ORD IDord-00f63dc131164864b60e46f64b514ffb
Source noteuspto-grants-1978_08