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Tetrahydro-2,8,4,6-(epoxyethanediylideneoxy)[1,3]dioxino[5,4-d]-1,3-dioxin synthesis

4synthesis methods
98510-20-4 Synthesis
1,3,5-O-METHYLIDYNE-MYO-INOSITOL

98510-20-4
41 suppliers
$145.00/1g

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Yield:-

Steps:

Multi-step reaction with 7 steps
1: 48 percent / imidazole / dimethylformamide / 24 h / 0 - 20 °C
2: 1.) NaH / 1.) DMF, 30 min, 2.) DMF, 24 h
3: tetrabutylammonium fluoride / tetrahydrofuran / 30 h
4: (COCl)2, DMSO / CH2Cl2 / 1 h
5: NaBH4 / methanol; tetrahydrofuran / 0.33 h
6: 94 percent / H2 / 20percent Pd(OH)2/C / tetrahydrofuran / 3 h / 2585.7 Torr
7: 100 percent / p-TsOH*H2O / tetrahydrofuran / 5 h / Ambient temperature

References:

Lee, Hyo Won;Kishi, Yoshito [Journal of Organic Chemistry,1985,vol. 50,# 22,p. 4402 - 4404]