HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369059Generated: October 28, 2026
Lithium diisopropylamide → 17-Difluoromethylene-7beta-methyl-3-tetrahydropyranyloxy-estra-1,3,5(10)-triene
https://huagongshe.com/reaction/369059
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | (Difluoromethyl)(oxo)diphenyl-lambda~5~-phosphane | HCID 15635908 | — |
| Reactant | 7beta-Methyl-3-tetrahydropyranyloxy-estra-1,3,5(10)-trien-17-one | HCID 18397084 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 17-Difluoromethylene-7beta-methyl-3-tetrahydropyranyloxy-estra-1,3,5(10)-triene | HCID 18397083 | — |
Reaction Steps
A solution of 2 g of difluoromethyldiphenylphosphine oxide in 55 ml of tetrahydrofuran is slowly mixed with 3.9 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 1.15 g of 7β-methyl-3-tetrahydropyranyloxy-estra-1,3,5(10)-trien-17-one in 20 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 2.5 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 is obtained as colorless crystals with a melting point of 85-86° C., [α]D22 =-59-4° (c=0.535% 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-9104464ad15a4a029a275edb81d691a8 |
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| Source note | uspto-grants-2000_10 |
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