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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Carbon Dioxide | HCID 280 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 3-Bromo-2-hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene | HCID 11078647 | — |
| 반응물 | HCID 178418306 | HCID 178418306 | — |
| 용매 | Pentane | HCID 8003 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Hexyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl-carboxylic acid | HCID 11012551 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05726191 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-4d21f97b1712426ea5d91e06fbf86981 |
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| 출처 메모 | uspto-grants-1998_03 |
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