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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65403Generated: October 26, 2026

Dexamethasone → Dexamethasone 9,11-epoxide

https://huagongshe.com/reaction/65403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDexamethasoneHCID 5743—
Reactant17beta-Hydroxy-16-methylenepregna-1,4,9(11)-triene-3,20-dioneHCID 13578837—
ProductDexamethasone 9,11-epoxideHCID 11143226—

Reaction Steps

Dexamethasone (9α-fluoro-11β,17α,21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione) can also be prepared from 17β-hydroxy-16-methylenepregna-1,4,9(11)-triene-3,20-dione (VI) by first transforming it to 17α,21-dihydroxy-16-methylenepregna-1,4,9(11)-triene-3,20-dione 21-acetate as described above and next transforming it to 17α,21-dihydroxy-16α-methylpregna-1,4,9(11)-triene-3,20-dione 21-acetate by the process of U.S. Pat. No. 3,130,209. 17α,21-Dihydroxy-16α-methylpregna-1,4,9(11)-triene-3,20-dione 21-acetate is then epoxidized by means well known to those skilled in the art, see for example U.S. Pat. No. 3,980,778, Examples 2 and 7 to produce 9β,11β-epoxy-17α,21-dihydroxy-16α-methylpregna-1,4-diene-3,20-dione which is transformed to dexamethasone 21-acetate by the process of U.S. Pat. No. 3,007,932, Example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04614621
Source datasetuspto-grants-1986_09
ORD IDord-4462328e288a41b88b3174407a5f3ed7
Source noteuspto-grants-1986_09