Hydrochloric Acid → 1-Cyclohexyl-1-hydroxy-1-phenyl-7-bromohept-5-yn-2-one

温度

-10 °C

To a dry flask under argon was added 1,1,1,3,3,3-hexamethyldisilazane (11.6 g, 71.6 mmole) and 75 ml of THF. The solution was cooled to -10° C. and n-BuLi (19.8 g, 71.3 mmol) was added directly to the reaction mixture. The solution was stirred at -10° C. for 30 minutes. A solution of 1-cyclohexyl-1-phenyl-1-trimethylsilyloxypropan-2-one (21.99 g, 72.2 mmol) in dry THF (75 ml) was added dropwise over a period of 15 minutes and the reaction mixture was stirred at -10° C. After the solution had stirred for 1 hour 1,4-dibromo-2-butyne (59.9 g, 0.3 mole) was added directly to the reaction mixture and the mixture was stirred an additional hour. The reaction was stopped by the dropwise addition of a solution of glacial acetic acid (7 ml) in ether (20 ml). The solution was warmed to room temperature and ether (150 ml) was added. The solution was washed with water followed by a saturated aqueous sodium chloride solution. The ether layer was dried and concentrated to afford a brownish liquid. This oil was dissolved in 150 ml of methanol and 0.2 ml of concentrated hydrochloric acid was added. The solution was stirred at 40° C. for 30 minutes and cooled to room temperature. Water was then added until the solution became cloudy and then 150 ml of ether was added. The solution was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, and evaporated under vacuum to afford a yellowish brown oil. Purification on a silica column with a hexane:ethyl acetate solution (98:2 followed by 9:1) afforded an orange oil (16.1 g, 59.5%). NMR (CDCl3) δ7.6-7.2(m, 5H), 4.3(s, 1H), 3.8(t, 2H), 2.8-2.6 (m, 2H), 2.5-2.3(m, 2H), 1.9-1.1(m, 11H). IR (neat) 3461, 2234, 1705, 609 cm-1. TLC (silica, petroleum ether:ethyl acetate (95:5)) Rf=0.53.

1. stirringthe reaction mixture was stirred at -10° C
2. additionwas added directly to the reaction mixture
3. stirringthe mixture was stirred an additional hour
4. temperatureThe solution was warmed to room temperature
5. washThe solution was washed with water
6. dry with materialThe ether layer was dried
7. concentrationconcentrated
8. customto afford a brownish liquid
9. stirringThe solution was stirred at 40° C. for 30 minutes
10. temperaturecooled to room temperature
11. washThe solution was washed with a saturated aqueous sodium chloride solution
12. dry with materialdried over sodium sulfate
13. customevaporated under vacuum
14. customto afford a yellowish brown oil
15. customPurification on a silica column with a hexane

ORDレコード

ord-412ef14ce34b4132b87a6fea29aa2ff3

出典データセット

uspto-grants-1991_07

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05036107