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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84975생성일: 2026년 10월 24일

Triethylamine → Adamantane-1-ylmethyl bromodifluoroacetate

https://huagongshe.com/ko/reaction/84975

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Tricyclo(3.3.1.1'3,7)dec-1-ylmethanolHCID 64556—
반응물Bromodifluoroacetyl chlorideHCID 520892—
용매Diethyl EtherHCID 3283—
생성물Adamantane-1-ylmethyl bromodifluoroacetateHCID 4690081495%

반응 조건

온도0 °C

반응 단계

Into a 50-L reaction vessel, 476 g (3.18 mol, 1.11 eq) of 1-adamantanemethanol and 5.5 kg of diethyl ether were added. The resulting solution was suspended by stirring, followed by adding thereto 615 g (2.86 mol, 1.0 eq) of bromodifluoroacetyl chloride. The suspended solution was cooled down to 0° C. Then, 578 g (5.72 mol, 2.0 eq) of triethylamine was slowly dropped to the cooled suspended solution. This reaction solution was left, while stirring, until it reached room temperature. The reaction solution was further stirred for 1 hour at room temperature. Subsequently, the reaction solution was washed with 5 kg of water. The thus-obtained organic layer was washed with 5 kg of saturated sodium hydrogencarbonate solution, with 5 kg of saturated sodium chloride solution, and then, with 5 kg of water. The washed organic layer was dried with magnesium sulfate and subjected to solvent distillation. With this, 878 g of target bromodifluoroacetic acid adamantane-1-ylmethyl ester was obtained (yield: 95%, purity: 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846966B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4fce67bffe8f4b49ab3b92037c204409
출처 메모uspto-grants-2014_09