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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44126생성일: 2026년 10월 24일

Triethylamine → 2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethyl methacrylate

https://huagongshe.com/ko/reaction/44126

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-MethoxyphenolHCID 9015—
반응물Methacryloyl chlorideHCID 13528—
반응물2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanolHCID 58105967—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2-(2-(2-Methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethyl methacrylateHCID 5782874197%

반응 단계

165 g (584 mmol) of 2-(2-(2-methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanol, 2,000 mL of THF, 105 mL (754 mmol) of triethylamine, and 0.165 g (1,000 ppm) of p-methoxyphenol were added to and dissolved in a 2 L three-necked flask equipped with a thermometer, a cooling pipe, and a stirrer. Following completion of the dissolution, 62.7 mL (648 mmol) of methacryloyl chloride was gradually added thereto while cooling in an ice bath. The temperature of the resultant was then elevated to room temperature, and the resultant was stirred for 3 hours. Following the completion of the reaction, 1,000 mL of diethyl ether was added thereto, followed by washing with 200 mL of distilled water 5 times. Thereafter, the extraction liquid was concentrated, thereby obtaining 198 g of an objective substance (namely, a compound 3 having the following structure) in the form of a colorless liquid (yield: 97%, GC purity: 99%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541157B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ed19f7c11f3d4a8095282b42ad8ac6c4
출처 메모uspto-grants-2013_09