Boron trifluoride etherate → HCID 15859118, compound

HRID 1200171Notes

Reaction equation

HRID 1200171 reaction equation
O1[C:3]23[C@:16]([CH3:21])([CH:17]=[CH:18][C:19](=[O:20])[CH:2]12)[C@@H:15]1[C@H:6]([C@H:7]2[C@@:11]([CH2:13][CH2:14]1)([CH3:12])[C:10](=[O:22])[CH2:9][CH2:8]2)[CH2:5][C:4]3=[CH2:23].B(F)(F)[F:25].CCOCC>C(OCC)C>[F:25][C:2]1[C:19](=[O:20])[CH:18]=[CH:17][C@@:16]2([CH3:21])[C:3]=1[C:4](=[CH2:23])[CH2:5][C@@H:6]1[C@@H:15]2[CH2:14][CH2:13][C@@:11]2([CH3:12])[C@H:7]1[CH2:8][CH2:9][C:10]2=[O:22]

Participants

4

Procedure

A solution of 4,5-epoxy-6-methylenandrost-1-ene-3,17-dione (1.0 g) in diethyl ether (100 ml) was treated with boron trifluoride etherate (1.4 ml) for 3 hours at room temperature. Then the solution was washed with 5% sodium carbonate solution, water, dried (Na2SO4) and evaporated in vacuo. The residue was dissolved in pyridine (20 ml) and 0.4 ml of thionyl chloride were added at 0° C. After 5 minutes water was added and the product isolated with ether. The ether extracts were washed with 2N hydrochloric acid, water, dried (Na2SO4) and evaporated. The resulting raw product was chromatographed on silica gel using hexane/ethyl acetate as eluant to yield 0.6 g of pure 4-fluoro-6-methylenandrosta-1,4-diene-3,17-dione.

Workup

  1. washThen the solution was washed with 5% sodium carbonate solution, water
  2. dry with materialdried (Na2SO4)
  3. customevaporated in vacuo
  4. dissolutionThe residue was dissolved in pyridine (20 ml)
  5. addition0.4 ml of thionyl chloride were added at 0° C
  6. additionAfter 5 minutes water was added
  7. customthe product isolated with ether
  8. washThe ether extracts were washed with 2N hydrochloric acid, water
  9. dry with materialdried (Na2SO4)
  10. customevaporated
  11. customThe resulting raw product was chromatographed on silica gel

Sources & evidence

ORD record
ord-0e6996fd772d4b45aae14cfa54152f39
Source dataset
uspto-grants-1990_02
Patent number
US04904650

Reaction notes

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