Реакция #10992

ord-16cdca0fbdee4983a28bd5c0535e7bcf

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Ethyl 2-(5-chloro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate was prepared (171 mg, 34%) in the same manner as described in the above example 6 (20) from ethyl 3-(5-chloro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate (0.45 g, 1.22 mmol) and p-toluenesulfonic acid monohydrate (50 mg), and the obtained product was identified with the following NMR data.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07094908B2uspto-grants-2006_08