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HRID 1245생성일: 2026년 10월 23일

Isobutyric Acid → 5-Bromo-5-chloro-4-(1,1-dimethoxyethoxy)-2-methyl-6,6,6-trifluorohex-2-ene

https://huagongshe.com/ko/reaction/1245

반응식

참여 물질

역할이름HCID투입량
반응물Isobutyric AcidHCID 6590—
반응물Trimethyl orthoacetateHCID 15050—
반응물1,1,1-Trifluoro-2-bromo-2-chloro-5-methyl-4-hexen-3-olHCID 15219346—
생성물5-Bromo-5-chloro-4-(1,1-dimethoxyethoxy)-2-methyl-6,6,6-trifluorohex-2-eneHCID 15278702—

반응 조건

온도111 °C

반응 단계

5-Bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene (10.0 g), trimethyl orthoacetate (48.0 g) and isobutyric acid (0.29 g) were charged to a round-bottomed flask fitted with: nitrogen inlet/bubbler, thermometer and Dean and Stark received packed with 5A molecular seives. The mixture was heated with agitation to reflux and distillates collected until reaction mass temperature increased to 111° C. (ca. 1 hr). Once the reaction was complete, the residual trimethyl orthoacetate was removed by distillation under vacuum (ca. 50° C. @ 50 mmHg) to give the product, 5-bromo-5-chloro-4-(1,1-dimethoxyethoxy)-2-methyl-6,6,6-trifluorohex-2-ene, as an orange oil (10.9 g, 85% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723649
출처 데이터셋uspto-grants-1998_03
ORD IDord-08430d7f4e5041b2a041747d195c0a59
출처 메모uspto-grants-1998_03