Sodium, 2,4-cyclopentadien-1-yl- → 3-Butenylcyclopentadiene

温度

0 °C

To a solution of 25.0 g (110 mmol) 3-buten-1-tosylate prepared according to step (a) above in 200 ml THF cooled to 0° C. was added 68.9 ml of 2.0M (138 mmol) sodium cyclopentadienylide in THF. The reaction mixture was allowed to warm to room temperature and was stirred for 16 h. 100 ml concentrated aqueous saline solution was added and the product extracted with ether (3×75 ml). The combined organic fractions were dried over magnesium sulphate for 2 hours, filtered and the solvents removed under reduced pressure using a rotary evaporator to yield a dark brown oil. The crude product was distilled under reduced pressure (b.p. 50°-51° C. @ 15 mm Hg) to give 5.71 g of a colourless oil (47.6 mmol, 43.3%).

1. temperatureto warm to room temperature
2. extractionthe product extracted with ether (3×75 ml)
3. dry with materialThe combined organic fractions were dried over magnesium sulphate for 2 hours
4. filtrationfiltered
5. customthe solvents removed under reduced pressure
6. customa rotary evaporator
7. customto yield a dark brown oil
8. distillationThe crude product was distilled under reduced pressure (b.p. 50°-51° C. @ 15 mm Hg)

ORDレコード

ord-c2b2e72518da4fc9be061b3544cf7db8

出典データセット

uspto-grants-1998_02

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05714425