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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1634생성일: 2026년 10월 23일

Carbon Dioxide → 3-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl-carboxylic acid

https://huagongshe.com/ko/reaction/1634

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물Hydrochloric AcidHCID 313—
반응물3-Bromo-2-hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthaleneHCID 11078647—
반응물HCID 178418306HCID 178418306—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물3-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl-carboxylic acidHCID 11012551—

반응 조건

온도-78 °C

반응 단계

15 g of 6-bromo-7-hexyl-1,1,4,4-tetramethyl-1, 2,3,4-tetrahydro-naphthalene were dissolved in 180 ml of tetrahydrofuran and treated dropwise at -78° C. with 64.5 ml of a 1.5 molar solution of tert.butyl-lithium in pentane. After stirring at -78° C. for 1 hour, a carbon dioxide stream was conducted vigorously into the reaction vessel for 2 hours. Subsequently, the reaction mixture was acidified by the addition of 190 ml of 2N hydrochloric acid, extracted several times with ethyl acetate, washed with water, dried over sodium sulfate and evaporated. The oily crude product was filtered over silica gel (eluent hexane, then hexane/ethyl acetate=4:1) and recrystallized from hexane. There were obtained 7.6 g of 3-hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl-carboxylic acid in colorless crystals, m.p. 98°-99° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726191
출처 데이터셋uspto-grants-1998_03
ORD IDord-4d21f97b1712426ea5d91e06fbf86981
출처 메모uspto-grants-1998_03