HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49413Generated: October 29, 2026
Methyl iodide → HCID 69625236, compound
https://huagongshe.com/reaction/49413
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | (7alpha,14beta,15beta)-3-Methoxy-7-methyl-14,15-methyleneestra-1,3,5 (10)-trien-17-one | HCID 69625115 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69625236 | HCID 69625236 | — |
Reaction Steps
i)—A solution of lithium bis(trimethylsilyl)amide (20.2 mmol) in tetrahydrofuran (35 ml) was cooled to −40° C. A solution of (7α,14β,15β)-3-methoxy-7-methyl-14,15-methyleneestra-1,3,5 (10)-trien-17-one (Example 1, step ii; 5.60 g) in dry tetrahydrofuran (24 ml) was added dropwise and the reaction mixture was stirred for 30 min. Then, at −30° C., iodomethane (2.4 ml) was added and stirring was continued for 45 min. The mixture was poured into a saturated aqueous solution of ammonium chloride and the product was extracted into ethyl acetate. The combined organic phases were washed with brine, dried over sodium sulfate and concentrated under reduced pressure, to give (7α,14β,15β,16α)-3-methoxy-7,16-dimethyl-14,15-methyleneestra-1,3,5(10)-trien-17-one (5.99 g). The product was used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706700B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-f9779105384c406b97e6f50f7bc6b266 |
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| Source note | uspto-grants-2004_03 |
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