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HRID 1270664作成日:2026年10月27日

Tricyclohexylphosphine → 5-Butylnorbornene 5-norbornene-2-carboxylic acid butyl ester 5-norbornene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1270664

反応式

関与物質

役割名称HCID仕込み量
反応物TricyclohexylphosphineHCID 75806—
反応物Bicyclo[2.2.1]hept-2-ene, 5-butyl-HCID 168020—
反応物Methyl bicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 250075—
反応物N,N-dimethylanilinium tetrakis(pentafluorophenyl)borateHCID 10996402—
反応物Butyl bicyclo[2.2.1]hept-5-ene-2-carboxylateHCID 15608148—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物5-Butylnorbornene 5-norbornene-2-carboxylic acid butyl ester 5-norbornene-2-carboxylic acid methyl esterHCID 86600019—

反応条件

温度90 °C

反応手順

5-Butylnorbornene (9.8 kg), 5-norbornene-2-carboxylic acid butyl ester (8.5 kg) and 5-norbornene-2-carboxylic acid methyl ester (16.7 kg) were added to a reactor at room temperature. Toluene (26.3 kg) was added to the reactor. Air inside the reactor was replaced by nitrogen and the reactor was heated to 90° C. Palladium diacetate (6.2 g), dimethyl aniliniumtetrakis (pentafluorophenyl)borate (44.1 g) and tricylcohexylphosphine (7.7 g) dissolved in dichloromethyl were added to the reactor. Reaction was performed for 18 hours while stirring to obtain a tricopolymer solution comprising 30 mol % of 5-butylnorbornene, 20 mol % of 5-norbornene-2-carboxylic acid butyl ester and 50 mol % of 5-norbornene-2-carboxylic acid methyl ester monomers. 43.9 kg of toluene was added to dilute the solution.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07202312B2
出典データセットuspto-grants-2007_04
ORD IDord-7d9d09ca1ae54b189c048f595094b186
出典メモuspto-grants-2007_04