HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369062Generated: October 28, 2026
Lithium diisopropylamide → 17-Difluoromethylene-3-tetrahydropyranyloxy-8alpha-estra-1,3,5(10)-triene
https://huagongshe.com/reaction/369062
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 3-Tetrahydropyranyloxy-8alpha-estra-1,3,5(10)-trien-17-one | HCID 15618136 | — |
| Reactant | (Difluoromethyl)(oxo)diphenyl-lambda~5~-phosphane | HCID 15635908 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 17-Difluoromethylene-3-tetrahydropyranyloxy-8alpha-estra-1,3,5(10)-triene | HCID 15308502 | 59.3% |
Reaction Steps
A solution of 3.5 g of difluoromethyldiphenylphosphine oxide in 100 ml of tetrahydrofuran is slowly mixed with 7 ml of 2 M lithium diisopropylamide solution at a bath temperature of =50° C., and it is stirred for 1 hour. Then, a solution of 2 g of 3-tetrahydropyranyloxy-8α-estra-1,3,5(10)-trien-17-one in 50 ml of tetrahydrofuran is slowly added, stirred for 15 minutes, slowly heated at a bath temperature of from -50° C. to 100° C. and refluxed for 2 hours. For working-up, it is diluted with ethyl acetate and water, suctioned off on Celite, rewashed with ethyl acetate, washed with water as well as with saturated sodium chloride solution, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/ethyl acetate/triethylamine. 1.3 g of 17-difluoromethylene-3-tetrahydropyranyloxy-8α-estra-1,3,5(10)-triene is obtained as colorless crystals with a melting point of 90-91° C., [α]D22 =-9.2° (c=0.5% in pyridine).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06136800 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-cf9b2dde5ab145cf9c406b556fc01bd7 |
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| Source note | uspto-grants-2000_10 |
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