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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256003생성일: 2026년 10월 25일

Ammonia → 1-(2-Hydroxyphenyl)-oct-1-yne

https://huagongshe.com/reaction/256003

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물1-IodohexaneHCID 12527—
반응물Lithium amideHCID 24532—
반응물2-EthynylphenolHCID 138415—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Hydroxyphenyl)-oct-1-yneHCID 1350025980%

반응 단계

To a grey suspension of lithium amide [lithium shot, (0.59 g, 0.085M) in liquid ammonia (250 ml)] at -30° C. was added 2-hydroxyphenyl acetylene (50 g, 0.042M, prepared by the method of G. A. Russell et al, J. Org. Chem. 31, 248 (1966)) in dry tetrahydrofuran (50 ml). The solution was stirred at reflux for 1 h, then iodohexane (8.91 g, 0.042M), in dry tetrahydrofuran (50 ml) was added dropwise. The reaction was refluxed for 6 h, then the ammonia allowed to evaporate overnight. The resultant pale brown solution was refluxed for 18 h, then cooled and poured into water. Acidified with dilute sulphuric acid and extracted into diethyl ether (twice). The combined organic phases were washed with water (twice), saturated brine and dried (MgSO4). Evaporation in vacuo yielded a red oil which was purified by distillation to give 6.80 g (80%) of the product as a colourless oil. νmax (film) 1463, 1485, 1575, 1608 (weak), 2225 (weak), 3500 cm-1, δ(CDCl3) 0.89 (3H, distorted t, terminal CH3) 1.40 (8 H, m, alkylene chain), 2.43 (2H, t, J 7 Hz, acetylenic CH2), 5.80 (1H, s, OH), 6.87 (2H, m, aromatics) 7.22 (2H, m, aromatics).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04699995
출처 데이터셋uspto-grants-1987_10
ORD IDord-a3e0ca1f479047beb36a4096426ff7fe
출처 메모uspto-grants-1987_10