Process for preparing α, α-dialkyl-α-hydroxymethyl-carboxylic acid derivatives
View Patent ↗The invention relates to a novel process for hydroxymethylating noncyclic α,α-dialkylcarboxylic acid derivatives with formaldehyde using amide bases at temperatures of from −40° C. up to the boiling point of the solvent or solvent mixture used.
1. A process for preparing α,α-dialkyl-α-hydroxymethylcarboxylic acid derivatives or salts thereof of the formula (II)
where
R 1 and R 2 are each independently selected from the group consisting of linear and branched alkyl radicals and aralkyl radicals,
R 3 is selected from the group consisting of hydrogen, optionally substituted linear and branched alkyl, aryl, aralkyl radicals, silyl radicals, alkali metal, alkaline earth metal, and amimonium,
R 4 is hydrogen, a hydroxyl protecting group, alkali metal or alkaline earth metal,
X is oxygen, where
R 5 is selected from the group consisting of hydrogen, linear or branched alkyl, aryl, aralkyl radicals and silyl radicals,
comprising: reacting α,α-dialkylcarboxylic acid derivatives or salts thereof of the formula (I)
with paraformaldehyde in the presence of an amide base in a solvent or solvent mixture at a reaction temperature of from −40° C. up to the boiling point of the solvent or solvent mixture.
2. The process of claim 1 , wherein the α,α-dialkylcarboxylic esters or α,α-dialkylcaiboxylic acids or salts thereof are compounds of the formula (I) where X is oxygen (O) and R 3 is selected from the group consisting of linear and branched alkyl, aryl, aralkyl, and silyl radicals.
3. The process of claim 2 , wherein X is oxygen (O) and R 3 is selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, benzyl and trimethylsilyl.
4. The process of claim 1 , wherein from 1 to 3 equivalents of the amide base based on α,α-dialkylcarboxylic acid derivative or salt thereof are used.
5. The process of claim 1 , wherein the solvent is selected from the group consisting of tetrahydrofuran, diethyl ether, MTBE, dibutyl ether, toluene, methylene chloride, pentane, hexane, heptane, petroleum ether, and mixtures thereof.
6. The process of claim 1 , wherein the amide base is a metal amide of the formula (III)
M(NR 6 R 7 ) n (III)
where
M is selected from the group consisting of lithium, sodium, potassium, magnesium and calcium,
R 6 and R 7 are each independently selected from the group consisting of hydrogen, linear and branched alkyl, aryl, aralkyl, and silyl radicals, and
n, depending on the valency of M, is 1 or 2.
7. The process of claim 1 , wherein the amide base is sodium hexamethyldisilazide, lithium hexamethyldisilazide, lithium diisopropylamide, or lithium tetramethylpiperidine.
8. The process of claim 1 , wherein the reaction is carried out at a temperature of from −30° C. to +60° C.
9. A process for preparing α,α-dialkyl-α-hydroxymethylcarboxylic acid derivatives of the formula (II)
where R 1 and R 2 are each independently selected from the group consisting of linear and branched alkyl radicals and aralkyl radicals,
R 3 is selected from the group consisting of optionally substituted linear and branched alkyl radicals, aryl radicals, aralkyl radicals, and silyl radicals,
R 4 is hydrogen, a hydroxyl protecting group, alkali metal or alkaline earth metal,
X is oxygen, where
R 5 is selected from the group consisting of hydrogen, linear or branched alkyl, aryl, aralkyl radicals and silyl radicals,
comprising: reacting α,α-dialkylcarboxylic acid derivatives of the formula (I)
with paraformaldehyde in the presence of an amide base in a solvent or solvent mixture at a reaction temperature of from −40° C. up to the boiling point of the solvent or solvent mixture.