Reacción #6053

ord-a3501c466ca1436bb389403a5114d62c

Ecuación de reacción

CC(C)(C)[Si](C)(C)OCC1CC(O)C1CO[Si](C)(C)C(C)(C)C
2,3-Bis(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)cyclobutanol
CC(C)(C)[Si](C)(C)OCC1CC(O)C1CO[Si](C)(C)C(C)(C)C
2.3-Bis(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)cyclobutanol
C[Si](C)(C)Cl
chlorotrimethyl-silane
OCC1CC(O)C1CO
title compound
OCC1CC(O)C1CO
2,3-Bis(hydroxymethyl)cyclobutanol

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónthen concentrated under reduced pressure to an oil
  2. 2
    OtroResidual chlorotrimethylsilane was removed by co-evaporation with methanol (3×30 mL)

Procedimiento

2,3-Bis(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)cyclobutanol (6.3 g, 17.5 mmol) from Step C was combined with 5.3 mL (43 mmol) of chlorotrimethyl-silane in 103 mL of methanol. The reaction mixture was stirred at ambient temperature under a nitrogen atmosphere for 0.5 h then concentrated under reduced pressure to an oil. Residual chlorotrimethylsilane was removed by co-evaporation with methanol (3×30 mL) to give title compound in quantitative yield and this crude product was carried on to the next step without purification; 1H NMR (CD3OD) δ 1.94-2.14 (m, 2H), 2.17-2.37 (m, 2H), 3.53 (d, 2H), 3.68 (dd, 1H), 3.85 (dd, 1H), 4.39 (m, 1H); MS DCI-NH3M/Z: 133 (M+H)+, 150 (M+NH4)+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05246931uspto-grants-1993_09