反応 #1069771

ord-d03077d8da2344eb9438ffc209efac2e

反応条件

温度
2.5°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The organic phase was separated
  2. 2
    洗浄rinsed with water, brine (×2)
  3. 3
    濃縮concentrated in vacuo
  4. 4
    その他to give a gum
  5. 5
    その他afforded 1.56 g (70%) of an off a white crystalline solid

実験手順

Compound 1b (2.0 g, 4.5 mmol) was dissolved in acetonitrile. Dimethylsulfide (6.6 mL) and acetic acid (2 mL) were added and the resulting mixture cooled to 0-5° C. (ice bath) under nitrogen. Benzoyl peroxide (6.36 g, 26 mmol) was added in several portions over 5 hours, then stirred for an additional 10 minutes, and then the reaction mixture was poured into a mixture of ethyl acetate and saturated aq. sodium bicarbonate (100 mL each). The organic phase was separated, rinsed with water, brine (×2), and concentrated in vacuo to give a gum. This gum upon addition of 50 mL of diethyl ether afforded 1.56 g (70%) of an off a white crystalline solid. m.p.=159-160° C. Spectral data were consistent with the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06861390B2uspto-grants-2005_03