Реакция #657256

ord-bd1d11566e3c49478fb26a962eb4c24c

Уравнение реакции

[H-].[Na+]
sodium hydride
COCCc1c(C)nn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1C
3,5-dimethyl-4-methoxyethyl-1-tritylpyrazole
COCc1cnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1
1-trityl-4-methoxymethylpyrazole
CCI
iodoethane
OCc1cnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1
1-trityl-4-hydroxymethylpyrazole
CCOCc1cnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c1
1-trityl-4-ethoxymethylpyrazole
Выход 87.0%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеhas been obtained

Методика

This compound is a slightly yellow solid and has been obtained as described in 2b for 1-trityl-4-methoxymethylpyrazole, starting from 1-trityl-4-hydroxymethylpyrazole (1.250 g; 3.67 mmol), sodium hydride (221 mg; 5.51 mmol) and iodoethane (1.5 mL; 18.35 mmol), as described in example 2a for 3,5-dimethyl-4-methoxyethyl-1-tritylpyrazole. Yield: 87% (1.174 g, 3.19 mmol).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09023315B2uspto-grants-2015_05