297156-50-4

Usage

Uses

Used in Pharmaceutical Industry:
2-Methyl-2-propenoic acid 2-(1-methylethyl)tricyclo[3.3.1.13,7]dec-2-yl ester is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical properties and reactivity allow for the creation of complex drug molecules, contributing to the development of new and innovative treatments.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Methyl-2-propenoic acid 2-(1-methylethyl)tricyclo[3.3.1.13,7]dec-2-yl ester serves as a crucial component in the production of various agrochemicals. Its versatility in forming complex structures enables the development of effective and targeted agrochemicals for crop protection and pest control.
Used in Specialty Chemicals:
2-Methyl-2-propenoic acid 2-(1-methylethyl)tricyclo[3.3.1.13,7]dec-2-yl ester is utilized in the manufacturing of specialty chemicals due to its unique chemical properties and reactivity. Its ability to form complex structures makes it a valuable component in the production of high-performance materials and advanced chemical products.
Used as a Flavor and Fragrance Ingredient:
Due to its unique chemical properties, 2-Methyl-2-propenoic acid 2-(1-methylethyl)tricyclo[3.3.1.13,7]dec-2-yl ester has potential applications as a flavor and fragrance ingredient. Its distinct characteristics can be harnessed to create novel and appealing scents and tastes in the flavor and fragrance industry.

Upstream product

• 38432-77-8 2-(propan-2-yl)adamantan-2-ol 
• 97-63-2 methyl methacrylate 
• 80-62-6 methacrylic acid methyl ester 
• 760-93-0 methacryloyl anhydride 
• 79-41-4 poly(methacrylic acid) 
• 700-58-3 2-Adamantanone 
• 75-29-6 isopropyl chloride 

Downstream Products

• 1422369-06-9 C₁₈H₁₅S⁽¹⁺⁾*C₁₉H₂₇F₂O₈S^(1-) 

Relevant academic research and scientific papers

Preparation method and device of 2-isopropyl-2-adamantanol (methyl) acrylate

The invention discloses a preparation method of 2-isopropyl-2-adamantanol (methyl) acrylate, and the method is characterized in that the 2-isopropyl-2-adamantanol (methyl) acrylate is prepared from (methyl) acrylate and isopropyl adamantane alcohol as reaction raw materials by taking an alkaline compound as a catalyst and carrying out ester exchange reaction at 40-120 DEG C in the presence of a solvent, wherein the alkaline compound catalyst is loaded on a porous carrier; the reaction liquid is filtered by a plate-type filter at 60-80 DEG C and then is cooled to a temperature of -60 DEG C to 0DEG C, and a separated solid is the 2-isopropyl-2-adamantanol (methyl) acrylate. According to the invention, the alkaline compound is used for loading a porous catalyst, the production process stepsare simple, the reaction is thorough, the yield is up to more than 95%, the purification process is simple, the purity of the product reaches more than 98%, the solvent and the catalyst can be recycled, the production cost is saved, and the preparation method realizes zero emission of pollutants, and is a green production method.

(Meth) acrylate compound adamantyl

PROBLEM TO BE SOLVED: To provide a method for obtaining, in a high recovery rate, an adamantyl (meth)acrylate compound of extremely high purity.SOLUTION: In the provided method for manufacturing an adamantyl (meth)acrylate compound, a crude adamantyl (meth)acrylate compound obtained by reacting a compound expressed by the following general formula (a) or (b) with (meth)acrylic acid, etc. is subjected either to first crystallization by using at least one type of water-soluble organic solvent and then to second crystallization by adding 100 to 1 pts.mass of water with respect to 100 pts.mass of the water-soluble organic solvent or to first crystallization by using a solvent mixture consisting of at least one type of water-soluble organic solvent and X to Y pts.mass of water with respect to 100 pts.mass of the water-soluble organic solvent and then to second crystallization by adding (100-X) to Z pts.mass of water.

METHOD FOR PRODUCING ADAMANTYL (METH)ACRYLATE COMPOUND

PROBLEM TO BE SOLVED: To provide a method for producing an adamantyl (meth)acrylate compound having an extremely high purity at a high recovery rate. SOLUTION: The method for producing an adamantyl (meth)acrylate compound comprises subjecting a crude adamantyl (meth)acrylate compound produced by reacting a compound represented by the general formula (a) as given below and (meth)acrylic acid or the like to a first crystallization using at least one kind of water-soluble organic solvent and then adding water in an amount of 100 to 1 pt.mass based on 100 pts.mass of the water-soluble organic solvent to subject the same to a second crystallization. (In the formula, R1 represents H or a 1-10C alkyl group; M represents H, an alkali metal or MgX (X is halogen).) SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

(Meth) acrylate hydroxyadamantyl

The present invention provides a method for producing an adamantyl (meth)acrylate, wherein a carboxylic acid ester compound is added into a reaction mixture that is obtained by the reaction of 1-adamantane carboxylic acid ester or 2-adamantanone with an organic metal compound, and then the resulting mixture is reacted with a (meth)acrylic acid anhydride. An adamantyl (meth)acrylate, which is suitable as a monomer for photoresist resins, is efficiently produced by this method.