反応 #2393692

反応方程式

26

(3-Buten-1-yl)[2-(2-methyl-1-propyl)-1,3-dithian-2-yl]diphenylsilane

water

→

ketone

収率 88.0%

1-[(3-Buten-1-yl)diphenylsilyl]-3-methyl-1 butanone

収率 88.0%

溶媒

CH3CN

反応条件

後処理

1. 1
   濃縮the mixture was concentrated
2. 2
   その他partitioned between water (100 mL) and hexane (200 mL)
3. 3
   その他The organic layer was isolated
4. 4
   抽出the aqueous layer extracted with hexane (50 mL)
5. 5
   洗浄The combined organic extracts were washed with saturated aqueous NaCl
6. 6
   その他dried over Na2 SO4
7. 7
   濃縮Concentration to dryness in vacuo at rt

実験手順

To a solution of 26 (4.64 g 11.2 mmol) in CH3CN (300 mL) was added water (10 mL) and HgCl2 (15.26 g, 56.21 mmol). After stirring overnight at rt, the mixture was concentrated and partitioned between water (100 mL) and hexane (200 mL). The organic layer was isolated and the aqueous layer extracted with hexane (50 mL). The combined organic extracts were washed with saturated aqueous NaCl and dried over Na2 SO4. Concentration to dryness in vacuo at rt gave crude ketone 33 as a yellow oil (3.2 g, 88%): Rf=0.80 (1/9 EtOAc:hexane); 1H NMR (300 MHz, CDCl3) δ 7.58 (d, J=6.4 Hz, 4H), 7.44 (m, 6H), 5.88 (m, 1H), 4.99 (dd, J=17.1, 1.6 Hz, 1H), 4.91 (dd, J=10.2, 1.6 Hz, 1H), 2.50 (d, J=6.6 Hz, 2H), 2.14 (m, 2H), 1.36 (m, 2H), 0.95 (m, 1H), 0.76 (d, J=6.7 Hz, 6H); IR (neat) 3068 (m), 3046(m), 2956(s), 2925 (m), 2864 (m), 1956(w), 1886(w), 1826(w), 1641 (s), 1471 (m), 1431 (s), 1113 (s), 1000 (m), 910 (m), 743 (s), 702 (s) cm−1; MS (FAB) m/e (rel. intensity) 323 (MH+, 15), 322 (24), 321 (89), 267, (17), 236 (36), 198 (20), 182 (63), 169 (100), 167 (15), 159 (31); HRMS (FAB) calcd for C21H25OSi: 321.1675 (H+−2), found: 321.1670.

出典