반응 #55570

ord-e7c5f52d7e334538a14be7fc7523ef98

반응 방정식

Cc1ccccc1C
xylene
[Na]
Sodium
Cc1ccccc1C
xylene
CCOC(=O)CC(=O)OCC
diethyl malonate
Cc1ccccc1C
xylene
O
water
CCOC(=O)C1(C(=O)OCC)CC(CC)C1
title compound
CCOC(=O)C1(C(=O)OCC)CC(CC)C1
3-Ethyl-1,1-dicarbethoxycyclobutane

반응 조건

온도
130°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to react at 120° C
  2. 2
    온도This reaction mixture was heated to about 150° C.
  3. 3
    온도The mixture was cooled
  4. 4
    추출extracted with 600 ml (3×300 ml) of ether
  5. 5
    추출extracted with 600 ml (2×300 ml) of ether
  6. 6
    추출The combined ether extract
  7. 7
    세척was washed with 200 ml of saturated aqueous sodium chloride
  8. 8
    건조dried over anhydrous magnesium sulfate
  9. 9
    여과filtered
  10. 10
    기타the solvent was removed in vacuo
  11. 11
    workup.DISTILLATIONDistillation of the product at reduced pressure

실험 절차

Sodium metal (7.6 g, 0.33 g/atom) was dispersed in 50 ml of dry xylene (distilled from sodium hydride) by heating to 130° C. with rapid stirring. Dry xylene (168 ml) and 47.8 g (45.2 ml, 0.298 mole) of diethyl malonate were then added thereto and the mixture was allowed to react at 120° C. To the resultant mixture there was then added 48.1 g (0.116 mole) of 2-ethyl-propyl-1,3-ditosylate (prepared in 1B) dissolved in 120 ml of dry xylene. This reaction mixture was heated to about 150° C. and stirred for 18 hr. The mixture was cooled and poured into 500 ml of water and extracted with 600 ml (3×300 ml) of ether. The aqueous material was made acidic with 10% aqueous HCl and then extracted with 600 ml (2×300 ml) of ether. The combined ether extract was washed with 200 ml of saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and the solvent was removed in vacuo. Distillation of the product at reduced pressure yielded 7.0 g of the title compound having the following physical characteristics:

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04220795uspto-grants-1980_09