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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476367Generated: October 30, 2026

Hexane → HCID 131732794, compound

https://huagongshe.com/reaction/1476367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantHCID 131732795HCID 131732795—
CatalystPalladiumHCID 23938—
SolventTolueneHCID 1140—
ProductHCID 131732794HCID 13173279490%

Reaction Steps

Using 7-methoxy-2-naphthyltrifluoromethanesulfonate (30.63 g, 0.10 mol) and 1-octyne (13.78 g, 0.125 mol), 7-octyn-1-yl-2-methoxynaphthalene was synthesized by the same operation as that in the method for synthesizing 7-decyl-2-methoxynaphthalene according to Example 3, and subjected to column chromatography (silica gel, developed with a mixture of toluene and hexane) to obtain a light yellow oil product of 7-octyn-1-yl-2-methoxynaphthalene (22.9 g, yield of 86%). The obtained 7-octyn-1-yl-2-methoxynaphthalene (total amount) was subjected to catalytic reduction in toluene (213 ml) under a hydrogen atmosphere by adding 10% Pd/C (2.13 g). The obtained product was subjected to column chromatography (silica gel, developed with a mixture of toluene and hexane) to obtain 7-octyl-2-methoxynaphthalene (compound (3)-10, 24.30 g, yield of 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018630B2
Source datasetuspto-grants-2015_04
ORD IDord-f1234b5c9fd64b81b7cd62a9ff4ca747
Source noteuspto-grants-2015_04