Abstract:
A process for producing an alkyl 3-(4-tetrahydropyranyl)-3-oxopropionate compound represented by the formula (1): (1) (wherein R1 and R2 may be the same or different and each represents a group not participating in the reaction, provided that R1 and R2 may be bonded to each other to form a ring optionally containing a heteroatom therein; and R3 represents a hydrocarbon group), characterized by reacting a 4-acyltetrahydropyran represented by the formula (2): (2) (wherein R1 and R2 have the same meanings as defined above) with a carbonic diester represented by the formula (3): (3) (wherein R3 has the same meaning as defined above, provided that the two R3's may be bonded to each other to form a ring) in the presence of a base. Also provided is a process for producing the 4-acyltetrahydropyran.
Abstract:
A method for producing a nitrile compound, a carboxylic acid compound or a carboxylate compound represented by the general formula (2): (2) (wherein R, R and R are as defined below) is characterized in that an acetic acid compound represented by the general formula (1) (wherein R represents a cyano group, a carboxyl group or an ester group; R and R respectively represent a group which may have a substituent and does not take part in the reaction; and R and R may combine together to form a ring) is decarboxylated in the presence of a metal catalyst.
Abstract:
A process for producing tetrahydropyran-4-ol, characterized by comprising: a cyclization step in which 3-buten-1-ol, a formaldehyde compound, and formic acid are reacted to form tetrahydropyranyl 4-formate, which is represented by the formula (1); (1) and a solvolysis step in which the tetrahydropyranyl 4-formate is solvoyzed to form tetrahydropyran-4-ol, which is represented by the formula (2).
Abstract:
Quinazolin-4-one or a derivative thereof is reacted with a chlorinating agent in a first organic solvent in the presence of an organic base. Subsequently, the reaction product is reacted with an amine compound represented by the formula R5-NH-R6 (R5 and R6 each represents hydrogen or an optionally substituted hydrocarbon group) in the presence of a second organic solvent. Thus, a 4-aminoquinazoline derivative can be obtained.
Abstract:
A process for producing a quinazolin-4-one derivative represented by the following formula (2): (2) (wherein R1, R2, R3, and R4 each represents a group not participating in the reaction and R1, R2, R3, and R4 may be bonded to each other to form a ring) which comprises reacting an anthranilic acid derivative represented by the following formula (1): (1) (wherein R5 represents hydrogen or a hydrocarbon group) with a formic acid derivative in the presence of an ammonium carboxylate.