Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188213Generated: October 29, 2026

Cyclohexanol → HCID 18477124, compound

https://huagongshe.com/reaction/2188213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 18477100HCID 18477100—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18477124HCID 18477124—

Reaction Steps

To a mixture of 2-(N-benzylmethylamino)methyl-6-hydroxy-1-phenyl-3,4-dihydronaphthalene (0.53 g), cyclohexanol (0.26 cm3), triphenylphosphine (0.579 g) and tetrahydrofuran (20 cm3), was added diethyl azodicarboxylate (0.35 cm3) at room temperature. After stirring for 5 h the solvent was removed under reduced pressure. The crude product was purified by column chromatography [silica, eluting with ethyl acetate-heptane (1:4)] to yield the title compound (0.442 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410592B1
Source datasetuspto-grants-2002_06
ORD IDord-5083437a1cd440759af9fe86620f3e62
Source noteuspto-grants-2002_06