| Identification | Back Directory | [Name]
(R)-(+)-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL | [CAS]
173831-50-0 | [Synonyms]
-2,2'-Bis(methoxymethoxy)
(R)-(+)-2,2'-Bis(methoxymethox
(R)-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAP&
2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL
2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHALENE
R-2,2'-Bis(methoxymethoxyl)-1,1'-binaphthyl
(R)-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL
(S)-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL
1,1'-Binaphthalene, 2,2'-bis(MethoxyMethoxy)-
(1R)-2,2'-Bis(MethoxyMethoxy)-1,1'-binaphthalene
(S)-(-)-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL
(R)-(+)-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHYL
(S)-(-)-2,2'-BIS(METHOXYMETHOXY)-1,1-BINAPHTHALENE
(R)-(+)-2,2'-BIS(METHOXYMETHOXY)-1,1'-BINAPHTHALENE
(R)-(+)-2,2'-Bis(methoxymethoxy)-1,1'-binaphthyl,98%
(R)-2,2'-Bis(methoxymethoxy)-1,1'-binaphthyl, 99%e.e. | [Molecular Formula]
C24H22O4 | [MDL Number]
MFCD03788935 | [MOL File]
173831-50-0.mol | [Molecular Weight]
374.43 |
| Chemical Properties | Back Directory | [Melting point ]
92-96 °C(lit.)
| [alpha ]
+85° (c 0.22, CHCl3) | [Boiling point ]
477.8±45.0 °C(Predicted) | [density ]
1.182±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Room Temperature | [solubility ]
soluble in Toluene | [form ]
Powder | [color ]
white | [Optical Rotation]
[α]20/D +92°, c = 1% in chloroform | [InChI]
1S/C24H22O4/c1-25-15-27-21-13-11-17-7-3-5-9-19(17)23(21)24-20-10-6-4-8-18(20)12-14-22(24)28-16-26-2/h3-14H,15-16H2,1-2H3 | [InChIKey]
YIAQRNNJNMLGTP-UHFFFAOYSA-N | [SMILES]
COCOc1ccc2ccccc2c1-c3c(OCOC)ccc4ccccc34 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless solid | [Uses]
An intermediate in the symmetric synthesis of BINOL-terpyridine ligands. | [Synthesis]
Sodium hydride (NaH, 1.92 g, 80 mmol) was slowly added to N,N-dimethylformamide (DMF, 30 mL) under ice bath conditions. Subsequently, a tetrahydrofuran (THF, 50 mL) solution of 1,1'-bi-2-naphthol (BINOL, 10 g, 34 mmol) was added slowly dropwise to the above mixture for 20 min. after 30 min, chloromethyl methyl ether (6.4 g, 80 mmol) was added slowly dropwise for the same period of time. The reaction process was monitored by thin layer chromatography (TLC). The reaction mixture was extracted with chloroform and water after stirring for 1 h. The organic layer was separated to obtain the crude product. The crude product was further purified by silica gel column chromatography with petroleum ether/ethyl acetate (5:1, v/v) as eluent. Finally, (R)-2,2'-bis(methoxymethoxy)-1,1'-binaphthyl was obtained in 90% yield. The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 7.95-7.93 (d, J = 9.6 Hz, 2H), 7.87-7.85 (d, J = 8.4 Hz, 2H), 7.58-7.56 (d, J = 9.6 Hz, 2H), 7.35-7.31 (m, 2H), 7.23-7.14 (m, 4H ), 5.08-4.96 (q, J = 6.8 Hz, 4H), 3.13 (s, 6H). | [References]
[1] Organic Letters, 2004, vol. 6, # 16, p. 2701 - 2704
[2] Tetrahedron Asymmetry, 2002, vol. 13, # 19, p. 2161 - 2166
[3] Chemistry - A European Journal, 2018, vol. 24, # 48, p. 12607 - 12612
[4] Chemistry Letters, 1995, # 12, p. 1113 - 1114
[5] Organic Preparations and Procedures International, 1995, vol. 27, # 6, p. 685 - 690 |
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