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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464704Generated: October 31, 2026

1-Naphthol → 1-(1-Naphthyl)-2-naphthol

https://huagongshe.com/reaction/1464704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphtholHCID 7005—
ReactantButanediaMide, 2,3-dihydroxy-, (R*,R*)-(±)-HCID 36689902—
Product1-(1-Naphthyl)-2-naphtholHCID 2755260—

Reaction Steps

On the other hand, 2.7 g of (+)-binaphthol (VII) ([α]D20, +21.0° (C=0.55, tetrahydrofuran)) which was obtained by silica gel chromatography of the filtrate obtained when the clathrate compound was separated and 2.19 g of (-)-(S,S)-tartaric acid diamide (X) were dissolved in the above-described mixed solvent, and thus-obtained solution was allowed to stand for 12 hours at room temperature. The crystallized crystal was recrystallized once to obtain 2.70 g of a clathrate compound (colorless prismatic crystal: mp, 150-151° C.; [α]D20, -43.9° (CHCl3)) containing (-)-tartaric acid diamide (X) and (+)-naphthol (XI) in a ratio of 1 : 1. The obtained crystal was subjected to column chromatography to obtain 1.48 g of (+)-binaphthol (VII) ([α]D20, +36.5° (C=1.3, tetrahydrofuran)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05306844
Source datasetuspto-grants-1994_04
ORD IDord-00dd28976e034ebbae195f643b4b9cce
Source noteuspto-grants-1994_04