تفاعل #67676

ord-31051ffd45274f689b1cc032228c745a

ظروف التفاعل

درجة الحرارة
-75°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGby stirring for 5 hours
  2. 2
    درجة الحرارةThe mixture was warmed to room temperature
  3. 3
    workup.STIRRINGby stirring for 30 minutes
  4. 4
    استخلاصextraction
  5. 5
    استخلاصThe aqueous layer was reversely extracted with ethyl acetate (1000 ml)
  6. 6
    غسيلwashed three times with a saturated sodium bicarbonate aqueous solution (1500 ml)
  7. 7
    تجفيفThe residue was dried over anhydrous magnesium sulfate
  8. 8
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

The crude compound 2-methyl-1-phenylpropan-2-yl 6-chloro-5-hydroxy-3-oxohexanoate (7a, 298 g) prepared in Example 1 was dissolved in a mixed solvent of tetrahydrofuran (2000 ml) and methanol (1000 ml), and the solution was cooled to −75° C. At the same temperature, methoxydiethylborane (78.8 ml) was gradually added dropwise to this solution over 20 minutes, followed by stirring for 40 minutes. Thereafter, sodium borohydride (25.0 g) was added in 5 divided portions, followed by stirring for 5 hours, and acetic acid (96 ml) was gradually added dropwise thereto. The mixture was warmed to room temperature and allowed to stand. Ethyl acetate (1800 ml) and a 3% hydrogen peroxide aqueous solution (1500 ml) were charged to the reaction section, followed by stirring for 30 minutes and extraction. The aqueous layer was reversely extracted with ethyl acetate (1000 ml), and the organic layer was combined and washed three times with a saturated sodium bicarbonate aqueous solution (1500 ml). The residue was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to give the crude title compound (13.6 g). A portion of the crude compound was purified by silica gel column (ethyl acetate:n-hexane=3:7(v/v)) to obtain the following NMR data.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524914B2uspto-grants-2013_09