Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthol | HCID 8663 | — |
| Solvent | Water | HCID 962 | — |
| Product | Binol | HCID 11762 | — |
Reaction Steps
Add 2 g 2-naphthol, 11.4 g FeCl3.6H2O and 100 ml water into a 200 ml beaker and agitate them at 65° C. by water bath; conduct TLC (thin-layer chromatography) track and maintain the reaction for 3 h; filter the solution to get solid 2,2′-dihydroxyl-1,1′-binaphthyl; scrub 2,2′-dihydroxyl-1,1′-binaphthyl with 50 ml water and add the cleaning solution into the filtrate; add 7.5 ml 30% H2O2 dropwise slowly into the filtrate while agitation and agitate the solution continuously for 10 min; add 2 g 2-naphthol and maintain the reaction at 65° C. while agitation; conduct TLC track until the reaction finishes; filter the solution to obtain 2,2′-dihydroxyl-1,1′-binaphthyl. Repeat these steps and obtain results as shown in Table 6. The HPLC analysis results of the reaction product obtained in the 11th time of cycle are: the conversion of 2-naphthol ≧98%, and the yield of 2,2′-dihydroxyl-1,1′-binaphthyl ≦99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964678B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-1a24d49c47024df19a09bb83898c84af |
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| Source note | uspto-grants-2011_06 |
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