Ethyl Bromide → n-Butyl 2-hydroxy-7-methyl-3-octynoate

온도

25 °C

A Grignard reagent was prepared under dry nitrogen by the addition, over a 1 hour period, of a solution comprising 10.9 grams (g) (0.10 mole) of ethyl bromide is 15 milliliters (ml) of anhydrous ether to a stirred suspension of 2.4 g (0.10 g atom) of clean magnesium metal turnings in 70 ml of dry ether. Stirring at 25° C. was continued for an additional hour and then a solution of 9.6 g (0.10 mole) of 5-methyl-1-hexyne in 15 ml of dry ether was added during 30 minutes with stirring. The resulting greyish solution was then heated at reflux for 2 hours and cooled to room temperature. The solution was transferred under dry nitrogen to a 200 ml addition funnel, followed by flushing with two 15 ml portions of dry ether. This solution was then added over a 45 minute period to a stirred solution of 13.0 g (0.10 mole) of n-butyl glyoxalate in 70 ml of dry ether cooled to -20° C. The mixture was stirred at -20° C. for 2 hours and allowed to warm to room temperature overnight. The resulting yellow-orange solution was cautiously treated with 75 ml of saturated ammonium chloride solution and after stirring for 5 minutes, the two phases which formed were separated. The aqueous phase was extracted twice with 60 ml portions of ether and the combined organic phases were washed with three 75 ml portions of brine and dried over MgSO4. After filtration and concentration at the stripper, the residual reddish-orange oil (18.0 g.), was fractionated through a 15 cm Vigreux column to afford, after a small forerun, a single volatile fraction, boiling point (b.p.) 107.0°-117.0° C./0.20 millimeter (mm). Redistillation of this cut provided 10.3 g (41% yield) of n-butyl 2-hydroxy-7-methyl-3-octynoate as a light yellow, sweet smelling, mobile oil, b.p. 112.0°-115.0° C./0.20 mm.

1. waitwas continued for an additional hour
2. stirringwith stirring
3. temperatureThe resulting greyish solution was then heated
4. temperatureat reflux for 2 hours
5. temperaturecooled to room temperature
6. additionThe solution was transferred under dry nitrogen to a 200 ml addition funnel
7. customby flushing with two 15 ml portions of dry ether
8. temperaturecooled to -20° C
9. stirringThe mixture was stirred at -20° C. for 2 hours
10. temperatureto warm to room temperature overnight
11. stirringafter stirring for 5 minutes
12. customthe two phases which formed
13. customwere separated
14. extractionThe aqueous phase was extracted twice with 60 ml portions of ether
15. washthe combined organic phases were washed with three 75 ml portions of brine
16. dry with materialdried over MgSO4
17. filtrationAfter filtration and concentration at the stripper
18. customto afford
19. custompoint (b.p.) 107.0°-117.0° C./0.20 millimeter (mm)
20. distillationRedistillation of this cut

ORD 기록

ord-974ee9d21cda4158964095703574db9d

출처 데이터셋

uspto-grants-1987_11

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US04704161