돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428222생성일: 2026년 10월 25일

1,1-Dibromoethane → 3-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propyne

https://huagongshe.com/reaction/428222

반응식

참여 물질

역할이름HCID투입량
반응물1,1-DibromoethaneHCID 11201—
반응물Ammonium ChlorideHCID 25517—
반응물1-Methoxypropa-1,2-dieneHCID 139403—
반응물6-Bromo-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthaleneHCID 226685—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물3-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propyneHCID 1777386947%

반응 조건

온도50 °C

반응 단계

20 g (0.82 mol) of magnesium activated with 0.1 ml of dibromoethane are introduced into a four litre reactor under a stream of nitrogen. A solution of 200 g (0.75 mol) of 2-bromo-5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene is added dropwise so as to maintain the reflux of the THF and the mixture is stirred at 50° C. for two hours. The reaction medium is then cooled to −5° C. and 1.2 g (8.2 mmol) of CuBr are added and a solution of 58 g (0.82 mol) of methoxyallene in 100 ml of THF is introduced dropwise. The mixture is stirred for one hour at −5° C. and is then allowed to return to room temperature and is stirred for two hours. The reaction medium is poured into saturated ammonium chloride solution and extracted with ethyl acetate, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. The oil obtained is distilled at 0.02 mm Hg and the fraction passing at 95-100° C. is collected. 79 g (47%) of the expected product are obtained in the form of a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313162B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-6c3aed9c74eb4c98968b6f85f068140e
출처 메모uspto-grants-2001_11