反応 #3996

ord-881c5b03087e4b6fa8b661db36b63481

反応方程式

O=C([O-])O.[Na+]
NaHCO3
CC(C=CC1=C(C)CCCC1(C)C)=CC=CC(C)=CC=C(C)CO
2,5,9-trimethyl-11-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8,10-undecapentaene-1-ol
COC(OC)OC
trimethyl orthoformate
CO
methanol
O=C(O)C(F)(F)F
trifluoroacetic acid
COCC(C)=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C
1-methoxy-2,5,9-trimethyl-11-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8,10-undecapentaene

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出extracted with chloroform three times
  2. 2
    抽出The combined organic extract
  3. 3
    洗浄is washed with water
  4. 4
    乾燥dried over Na2SO4
  5. 5
    その他evaporated in vacuo
  6. 6
    その他to give a residue, which
  7. 7
    その他is purified by HPLC (4% ether in hexane, silica gel column)

実験手順

To a solution of 2,5,9-trimethyl-11-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8,10-undecapentaene-1-ol (1.6 g, 5 mmol), 106 g (10 mmol) of trimethyl orthoformate and 160 mg (5 mmol) of dry methanol in 5 ml of dry THF is added dropwise a solution of 40 μL of trifluoroacetic acid in 1 ml of dry THF over a 1 minute period at room temperature. After overnight standing, the reaction mixture is poured into cold aqueous 5% NaHCO3 and extracted with chloroform three times. The combined organic extract is washed with water, dried over Na2SO4 and evaporated in vacuo to give a residue, which is purified by HPLC (4% ether in hexane, silica gel column) to afford of 1-methoxy-2,5,9-trimethyl-11-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8,10-undecapentaene as an oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04722939uspto-grants-1988_02