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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369793Generated: October 28, 2026

Cyclohexene → HCID 18968462, compound

https://huagongshe.com/reaction/369793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantTriethylamineHCID 8471—
Reactant2-Iodobenzylic alcoholHCID 107629—
SolventMethanolHCID 887—
ProductHCID 18968462HCID 1896846242%

Reaction Steps

According to example 61, 10.0 g of 2-iodobenzyl alcohol was treated with 25 mL of cyclohexene (Aldrich) using 0.96 g of Pd(O Ac)2, 2.60 g of tri-ortho-tolyphosphine, and 6.6 mL of Et3N at 100° C. for 48 h. The resulting olefin mixture was hydrogenated for 6.5 h using 0.36 g of 5% Pt(C) in MeOH to afford 3.37 g (42%) of 2-cyclohexyl benzyl alcohol as a light yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140100
Source datasetuspto-grants-2000_10
ORD IDord-96b7f96d77544fe2a7c284f7c33a8ecf
Source noteuspto-grants-2000_10