Method for deuteration of an aromatic ring
View Patent ↗The present invention relates to a method for deuteration of a compound having an aromatic ring, using an activated catalyst, and the method comprises reacting a compound having an aromatic ring with heavy hydrogen source in the presence of an activated catalyst selected from a platinum catalyst, a rhodium catalyst, a ruthenium catalyst, a nickel catalyst and a cobalt catalyst.
1. A method for deuteration of an aromatic ring comprising:
reacting the aromatic ring under a neutral condition with a deuterated solvent that is neither deuterium peroxide (D 2 O 2 ) nor supercritical D 2 O in the presence of only one activated catalyst under non-supercritical condition,
wherein the aromatic ring may have at least one substituent and is at least one selected from the group consisting of benzene, naphthalene, anthracene, phenanthrene, 9,10-dihydroanthracene, naphthacene, pentaphene, pentacene, hexaphene, hexacene, heptaphene, heptacene, trinaphthylene, 1,4-dihydronaphthalene, pyrene, triphenylene, biphenylene, indene, indan, indacene, phenalene, fluorene, acenaphthene, acenaphthylene, fluoranthene, tetraphenylene, coranthrene, acephenanthrylene, aceanthrylene, cyclopentaphenanthrene, chrysene, picene, pleiadene, rubicene, pyranthrene, coronene, perylene, rubrene, dibenzophenanthrene, 1,2-dibenzo-1,3-cycloheptadiene and ovalene,
the reaction is carried out at 180° C. or lower, and
the only one activated catalyst is activated platinum carbon and is activated with hydrogen or heavy hydrogen gas.
2. The method for deuteration according to claim 1 , wherein the activated platinum carbon catalyst is one comprising platinum with valence of 0 to 2.
3. The method for deuteration according to claim 1 , wherein the at least one substituent of the aromatic ring is selected from the group consisting of a halogen atom, a hydroxyl group, a mercapto group, an oxo group, a thioxo group, a carboxyl group, a sulfo group, a sulfino group, a sulfeno group, a phosphino group, a phosphinoyl group, a formyl group, an amino group, a cyano group and a nitro group.
4. The method for deuteration according to claim 1 , wherein the at least one substituent of the aromatic ring is selected from the group consisting of an alkyl group, an alkenyl group, an aryl group, an aralkyl group, an alkoxy group, an aryloxy group, an alkylthio group, an arylthio group, an alkylsulfonyl group, an arylsulfonyl group, an alkylsulfinyl group, an arylsulfinyl group, an alkylphosphino group, an arylphosphino group, an alkylphosphinoyl group, an arylphosphinoyl group, an alkylamino group, an arylamino group, an alkoxycarbonyl group, an aryloxycarbonyl group, an alkoxysulfonyl group, an aryloxysulfonyl group, an acyl group and an acyloxy group, which may further have at least one substituent.
5. The method for deuteration according to claim 4 , wherein the at least one substituent of the aromatic ring has at least one substituent selected from the group consisting of an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a hydroxy group, an alkoxy group, an amino group, an alkylamino group, a mercapto group, an alkylthio group, an formyl group, an acyl group, a carboxyl group, an alkoxycarbonyl group, a carbamoyl group and an alkylcarbamoyl group.
6. The method for deuteration according to claim 1 , where the deuterated solvent is at least one selected from the group consisting of deuterium oxide, deuterated alcohols, deuterated carboxylic acids, deuterated ketones, deuterated dimethylsulfoxide, and tritium oxide.