Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | ButanediaMide, 2,3-dihydroxy-, (R*,R*)-(±)- | HCID 36689902 | — |
| Product | 1-(1-Naphthyl)-2-naphthol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05306844 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-00dd28976e034ebbae195f643b4b9cce |
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| Source note | uspto-grants-1994_04 |
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