تفاعل #612798

ord-4e129029649944cda79d981eb838d78c

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصThe reaction mixture is extracted with ethylacetate (2×15 mL)
  2. 2
    تجفيفThe combined organics are dried over MgSO4
  3. 3
    ترشيحfiltered
  4. 4
    أخرىevaporated
  5. 5
    أخرىto give the crude product, which
  6. 6
    أخرىis purified by silica chromatography
  7. 7
    غسيلeluting from 25% ethylacetate/heptanes to neat ethylacetate

الإجراء التجريبي

Trifluoroacetic acid (51.6μL) is added to the product of step 3, Example 95A (0.168 g, 0.335 mmol) and pyridine (54.2μL, 0.67 mmol) in THF (4.4 mL, 54 mmol) at 0° C. After 5 minutes, bis(benzyloxy)(diisopropylamino)phosphine (0.219 mL, 0.586 mmol) is added. After allowing to warm to room temperature the mixture is stirred for 1 hour. 30% hydrogen peroxide/water (30:70, 60μL, 0.586 mmol) is added. After 1 hour sodium bisulfate (4 mL) is added and water (10 mL) is added. The reaction mixture is extracted with ethylacetate (2×15 mL). The combined organics are dried over MgSO4, filtered and evaporated to give the crude product, which is purified by silica chromatography eluting from 25% ethylacetate/heptanes to neat ethylacetate to give the title product (241 mg): m/z: 761.25.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09340564B2uspto-grants-2016_05