2-Chloro acid methyl esters were prepared in good yields treating 2-chloro aldehyde dimethyl acetals with trichloroisocyanuric acid in DMF. Aldehyde dimethyl acetals with the 2-halogen on a tertiary carbon atom were poorly reactive and could be oxidized effeciently only after their transformation into 1,3-dioxolanes.

TRICHLOROISOCYANURIC ACID OXIDATION OF 2-CHLORO ALDEHYDE ACETALS TO 2-CHLORO ACID-ESTERS / Boni, M; Ghelfi, Franco; Pagnoni, Ugo Maria; Pinetti, Adriano. - In: BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN. - ISSN 0009-2673. - STAMPA. - 67:(1994), pp. 156-159.

TRICHLOROISOCYANURIC ACID OXIDATION OF 2-CHLORO ALDEHYDE ACETALS TO 2-CHLORO ACID-ESTERS

GHELFI, Franco;PAGNONI, Ugo Maria;PINETTI, Adriano
1994

Abstract

2-Chloro acid methyl esters were prepared in good yields treating 2-chloro aldehyde dimethyl acetals with trichloroisocyanuric acid in DMF. Aldehyde dimethyl acetals with the 2-halogen on a tertiary carbon atom were poorly reactive and could be oxidized effeciently only after their transformation into 1,3-dioxolanes.
1994
67
156
159
TRICHLOROISOCYANURIC ACID OXIDATION OF 2-CHLORO ALDEHYDE ACETALS TO 2-CHLORO ACID-ESTERS / Boni, M; Ghelfi, Franco; Pagnoni, Ugo Maria; Pinetti, Adriano. - In: BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN. - ISSN 0009-2673. - STAMPA. - 67:(1994), pp. 156-159.
Boni, M; Ghelfi, Franco; Pagnoni, Ugo Maria; Pinetti, Adriano
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