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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2167155생성일: 2026년 10월 26일

Ethyl Bromide → 1-(1-Methoxyisopropoxy)pent-2-yne

https://huagongshe.com/reaction/2167155

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물IsopreneHCID 6557—
반응물Lithium amideHCID 24532—
반응물3-(1-Methoxy-1-methylethoxy)propyneHCID 3017891—
용매HexaneHCID 8058—
생성물1-(1-Methoxyisopropoxy)pent-2-yneHCID 3019831105.6%

반응 단계

259 mg (37 mmol) of granulated lithium were added within 5 minutes to 47.7 g (1.9 mol) of liquid ammonia at −40° C. The mixture was stirred until no more lithium floated (after approximately 10 minutes). A dark blue solution of lithium in liquid ammonia was obtained. 4.0 ml (40 mmol) of isoprene were added portion wise within 10 minutes. The end of the formation of lithium amide could be recognized by the discoloration of the reaction mixture. 2.9 g (20 mmol) of 3-(1-methoxy-1-methyl-ethoxy)-propyne (88.9% GC) were added with a dropping funnel to the reaction mixture at −40° C. within 20 minutes. The reaction mixture was held at −40° C. for about 1 hour. 8.9 g (80 mmol) of bromoethane were added with a dropping funnel to the reaction mixture within 10 minutes. The reaction mixture was subsequently stirred for 1 hour. 20 ml of n-hexane were added to the reaction mixture and the liquid ammonia was evaporated under normal pressure within 5 hours. 20 ml of water were added to the reaction mixture at 22° C., and the mixture was stirred until all salt was dissolved. The organic layer was separated and dried over 2 g of anhydrous magnesium sulfate. The solution was concentrated under reduced pressure (40° C., 40 mbar) and the crude product was analyzed by GC. 3.3 g of crude 1-(1-methoxy-1-methyl-ethoxy)-pent-2-yne were obtained with a purity of 75.6% (yield 80.0% based on 3-(1-methoxy-1-methyl-ethoxy)-propyne).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09045404B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-387a98b9f710405eb818df2beb47ca5a
출처 메모uspto-grants-2015_06