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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49413Generated: October 29, 2026

Methyl iodide → HCID 69625236, compound

https://huagongshe.com/reaction/49413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant(7alpha,14beta,15beta)-3-Methoxy-7-methyl-14,15-methyleneestra-1,3,5 (10)-trien-17-oneHCID 69625115—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69625236HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706700B2
Source datasetuspto-grants-2004_03
ORD IDord-f9779105384c406b97e6f50f7bc6b266
Source noteuspto-grants-2004_03