반응 #8640

ord-944f1193a82d4416b583f12b44d9cb7f

반응 방정식

C=CCC[Si](C)(c1ccccc1)C1(CC(C)C)SCCCS1
44
C=CCC[Si](C)(c1ccccc1)C1(CC(C)C)SCCCS1
(3-Buten-1-yl)methyl[2-(2-methyl-1-propyl)-1,3-dithian-2-yl]phenylsilane
O
water
C=CCC[Si](C)(C(=O)CC(C)C)c1ccccc1
ketone
C=CCC[Si](C)(C(=O)CC(C)C)c1ccccc1
1-[(3-Buten-1-yl)methylphenylsilyl]-3-methyl-1-butanone

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    농축the mixture was concentrated
  2. 2
    기타partitioned between water (100 mL) and hexane (200 mL)
  3. 3
    기타The organic layer was isolated
  4. 4
    추출the aqueous layer extracted twice with 50-mL portions of hexane
  5. 5
    세척The combined organic extracts were washed with saturated aqueous NaCl
  6. 6
    건조dried over Na2SO4

실험 절차

To a solution of 44 (6.19 g, 177 mmol) in CH3CN (200 mL) was added water (10 mL) and HgCl2 (24 g, 88 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 twice with 50-mL portions of hexane. The combined organic extracts were washed with saturated aqueous NaCl and dried over Na2SO4. Concennation to dryness in vacuo at rt gave quantitatively crude ketone 45 as a yellow oil. This ketone was used in the next reaction without further purification: Rf=0.75 (1/19 EtOAc:hexane); 1H NMR (300 MHz, CDCl3) δ 7.54–7.51 (m, 2H), 7.41–7.35 (m, 3H), 5.91–5.78 (m, 1H), 4.99 (dd, J=17.0, 1.7 Hz, 1H), 4.90 (dd, J=10.0, 1.7 Hz, 1H), 2.44 (d, J=6.7 Hz, 2H), 2.16–2.06 (m, 3H), 1.16–1.07 (m, 2H), 0.78 (pd. J=6.7 Hz, 6H), 0.51 (s, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087776B2uspto-grants-2006_08