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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1940생성일: 2026년 10월 24일

(4Z,7Z)-1-(tetrahydropyran-2-yloxy)-4,7-decadiene → 3E,8Z-Tetradecadienyl acetate

https://huagongshe.com/ko/reaction/1940

반응식

참여 물질

역할이름HCID투입량
반응물(4Z,7Z)-1-(tetrahydropyran-2-yloxy)-4,7-decadieneHCID 10966579—
반응물(4Z,7Z)-1-bromo-4,7-decadieneHCID 11106805—
반응물(8Z,11Z)-8,11-tetradecadien-1-yl acetateHCID 86752265—
생성물3E,8Z-Tetradecadienyl acetateHCID 10538786—

반응 단계

Dry THF (3 ml) was treated with trimethylsilyl iodide (260 mg, 185 μl, 1.30 mmol) at room temperature and stirred for 15 min to form 4-trimethylsiloxybutyl iodide (11). A solution of CuCN. (LiCl)2 in THF (1M, 100 μl) was added, and the mixture was cooled to -40° C. The above prepared solution of Grignard reagent 10, was then added over a period of 30 min, and a white precipitate formed. The mixture was stirred at -40° to -20° C. for 1 hr followed by an additional 1 hr at room temperature. The reaction was quenched with ammonium chloride solution and ammonia mixture (2:1, v/v), and the product was extracted with hexane/ether (1:1) mixture (Rf =0.60, 19:1 hexane/ethyl acetate, v/v). The crude (8Z,11Z)-trimethylsiloxy-8,11-tetradecadiene (12) was dissolved in THF (6 ml) and deprotected with tetrabutylammonium fluoride solution in THF (1M, 2 ml) to form the alcohol 13. Acetylation of the alcohol 13 with acetic anhydride/pyridine mixture (0.1 ml/1 ml) and purification by flash chromatography afforded (8Z,11Z)-8,11-tetradecadien-1-yl acetate (14) (80 mg) in 34% yield based on the starting bromide (5). 1H NMR (400 MHz) δ: 5.36 (m, 4H, CH=CH-8, 9, 11, 12), 4.05 (t, J=6.7, 7.0 Hz, 2H, CH2 -1), 2.77 (dd, J=6.4, 6.4 Hz, 2H, =CH--CH2 --CH=), 2.06 (m, 4H, CH2 -7, 13), 2.04 (s, 3H, --COCH3), 1.60 (tt, J=7.3, 7.3, 7.6, 7.6 Hz, 2H, CH2 -6), 1.4-1.2 (m, 8H, CH2 -2, 3, 4, 5), 0.97 (t, J=7.3, 7.6 Hz, 3H, CH3 -14). 13C NMR (100.6 MHz) δ: 171.2 (C=O), 131.7 (=CH-12), 130.0 (=CH-11), 128.0 (=CH-9), 127.3 (=CH-8), 64.6 (CH2 -1), 29.5 (CH2 -2), 29.1 (CH2 -3, 4), 28.6 (CH2 -5), 27.2 (CH2 -6), 25.9 (CH2 -7), 25.5 (CH2 -10), 21.0 (CH3C=O), 20.5 (CH2 -13), 14.3 (CH3). MS [EI, m/z(%)] 252 (M+,2), 209 (M+ -43, 1), 192 (M+ -60, 23), 163 (4); 149 (8), 135 (14), 121 (38), 110 (19), 107 (19), 95 (39), 93 (40), 82 (26), 81 (57), 79 (66), 67 (100), 55 (38), 43 (93), 41 (50). IR (gas phase, cm-1) 3017 (cis=C--H str), 2936 (CH2), 1761 (C=O), 1233, 1040 (--O--). (3E,8Z)-3,8-tetradecadienyl acetate was synthesized as described in detail below with reference to the following reaction sequence. ##STR17##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728376
출처 데이터셋uspto-grants-1998_03
ORD IDord-2b18349f92ab4ab2a31939346351aab8
출처 메모uspto-grants-1998_03