反应 #1435720

ord-a4528f76be924b91a658fcb1b32c97a0

反应方程式

[Cl-].[NH4+]
ammonium chloride
[Na+].c1cc[cH-]c1
sodium cyclopentadienylide
C[Si](C)(C)OCCCBr
3-bromo-1-trimethylsiloxypropane
C[Si](C)(C)OCCCC1=CC=CC1
(3-trimethylsiloxypropyl)-cyclopentadiene
收率 43.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The reaction is maintained
  2. 2
    萃取the organic phase is extracted
  3. 3
    浓缩concentrated to dryness in order
  4. 4
    其他to give an orange oil

实验过程

To 50 ml of a 2.3 M solution of sodium cyclopentadienylide (115 mmol), a solution of 24.3 g (115 mmol) of 3-bromo-1-trimethylsiloxypropane in tetrahydrofurane is added. The quick formation of a pinkish solid is observed. The reaction is maintained under stirring for 12 hours and then it is neutralised with an ammonium chloride solution; the organic phase is extracted and concentrated to dryness in order to give an orange oil. (9.8 g, 50 mmol. Yield: 43%). 1H-NMR (CDCl3): 6.47–6.00 (m, 3H), 3.62 (m, 2H), 2.95 (m, 1H), 2.87 (m, 1H), 2.43 (m, 2H), 1.80 (m, 2H), 0.17 (s, 9H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07211538B2uspto-grants-2007_05