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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476368Generated: October 30, 2026

Hexane → HCID 131732796, compound

https://huagongshe.com/reaction/1476368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantHCID 131732797HCID 131732797—
CatalystPalladiumHCID 23938—
SolventTolueneHCID 1140—
ProductHCID 131732796HCID 13173279696%

Reaction Steps

Using 7-methoxy-2-naphthyltrifluoromethanesulfonate (30.63 g, 0.10 mol) and 1-dodecyne (20.79 g, 0.125 mol), 7-dodecyn-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-dodecyn-1-yl-2-methoxynaphthalene (32.0 g, quantitative). The obtained 7-dodecyn-1-yl-2-methoxynaphthalene (total amount) was subjected to catalytic reduction in toluene (316 ml) under a hydrogen atmosphere by adding 10% Pd/C (2.11 g). The obtained product was subjected to column chromatography (silica gel, developed with a mixture of toluene and hexane) to obtain 7-dodecyl-2-methoxynaphthalene (compound (3)-14, 31.10 g, yield of 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018630B2
Source datasetuspto-grants-2015_04
ORD IDord-704b1a48b26c4b38a9973be475de8d89
Source noteuspto-grants-2015_04