Process for producing 4-hydroxycyclopentenones
AssigneeSumitomo Chemical Company, Limited
InventorsKenji Saito, Hiroshi Yamachika
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AssigneeSumitomo Chemical Company, Limited
InventorsKenji Saito, Hiroshi Yamachika
Estimating the term…
A method of producing a 4-hydroxycyclopentenone represented by the formula, ##STR1## wherein R.sub.1 is an alkyl, alkenyl, alkynyl, cycloalkyl, thienyl, phenyl, p-methylbenzyl or benzyl group and R.sub.2 is an alkyl, alkenyl or alkynyl group having 6 or less carbon atoms, which comprises reacting a furylcarbinol compound of the formula, ##STR2## wherein R.sub.1 is as defined above, in the presence of an acid in a mixed solvent of water and an organic solvent, to obtain a cyclopentenone compound of the formula, ##STR3## wherein R.sub.1 is as defined above; reacting the cyclopentenone compound in the presence of an oxidizing agent to obtain a cyclopentendione compound of the formula, ##STR4## wherein R.sub.1 is a defined above; reacting the cyclopentendione compound with a Grignard reagent of the formula, R.sub.2 MgX wherein R.sub.2 is as defined above and X is chlorine, bromine or iodine atom, to obtain an oxocyclopentene compound of the formula, ##STR5## wherein R.sub.1 and R.sub.2 are as defined above; and reacting the cyclopentenone compound in the presence of a base. The 4-hydroxycyclopentenones are useful intermediates of agricultural chemicals.
A method of producing a 4-hydroxycyclopentenone represented by the formula ##STR19## wherein R.sub.1 is an alkyl, alkenyl, alkynyl, cycloalkyl, thienyl, phenyl, p-methylbenzyl or benzyl group and R.sub.2 is an alkyl, alkenyl or alkynyl group having 6 or less carbon atoms, which comprises reacting a cyclopentendione compound of the formula, ##STR20## wherein R.sub.1 is as defined above, with a Grignard reagent of the formula,
A method of producing a 4-hydroxycyclopentenone represented by the formula, ##STR22## wherein R.sub.1 is an alkyl, alkenyl, alkynyl, cycloalkyl, thienyl, phenyl, p-methylbenzyl or benzyl group and R.sub.2 is an alkyl, alkenyl or alkynyl group having 6 or less carbon atoms, which comprises oxidizing a cyclopentenone compound of the formula, ##STR23## wherein R.sub.1 is as defined above, in the presence of an oxidizing agent selected from the group consisting of chromic anhydride, chromates, dichromic acid, dichromates, chromyl chloride, chromate esters, chromic oxide-pyridine complex, manganese dioxide, activated manganese dioxide, potassium permanganate, aluminum isopropoxide, aluminum tert-butoxide, lead tetraacetate, ruthenium tetraoxide, N-halocarboxylic acid amide, oxygen, hydrogen peroxide, organic peroxides, halogen, nitric acid, nitrous acid, dimethyl sulfoxide, quinones, silver (I) carbonate, silver (II) carbonate, copper (II) oxide, copper (II) hydroxide, cerium (IV) salts, vanadates, cobalt (II) salts and ozone, at -20.degree. to 180.degree. C., to obtain a cyclopentendione compound of the formula, ##STR24## wherein R.sub.1 is as defined above;
A method of producing a 4-hydroxycyclopentenone represented by the formula, ##STR26## wherein R.sub.1 is an alkyl, alkenyl, alkynyl, cycloalkyl, thienyl, phenyl, p-methylbenzyl or benzyl group and R.sub.2 is an alkyl, alkenyl or alkynyl group having 6 or less carbon atoms, which comprises reacting a furylcarbinol compound of the formula, ##STR27## wherein R.sub.1 is as defined above, in the presence of an acid selected from the group consisting of formic acid, trichloroacetic acid, dichloroacetic acid, phosphoric acid, polyphosphoric acid and pyrophosphoric acid, in a mixed solvent of water and an organic solvent selected from the group consisting of acetone, dioxane, methyl ethyl ketone, tetradyrofuran and dimethyl sulfoxide, to obtain a cyclopentenone compound of the formula, ##STR28## wherein R.sub.1 is as defined above;
Dependencies are inferred from the claim text.