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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918404Generated: October 29, 2026

Ethane, 2-diazo-1,1-diethoxy- → 6alpha-Fluoro-16alpha-[(2,2-diethoxy)ethoxy]-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dione

https://huagongshe.com/reaction/918404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthane, 2-diazo-1,1-diethoxy-HCID 21520892—
Reactant6alpha-Fluoro-11beta,16alpha,17,21-tetrahydroxypregna-1,4-diene-3,20-dioneHCID 22793229—
Product6alpha-Fluoro-16alpha-[(2,2-diethoxy)ethoxy]-11beta,17,21-trihydroxypregna-1,4-diene-3,20-dioneHCID 22791783—

Reaction Steps

A solution of 2,2-diethoxy-1-diazoethane (prepared from 0.18 mole of precursor as described in Example 2A) in methanolether at 0°C is treated with 6α-fluoro-11β,16α,17,21-tetrahydroxypregna-1,4-diene-3,20-dione, 16,17-cycloborate until nitrogen evolution ceases. The solution is evaporated to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03971773
Source datasetuspto-grants-1976_07
ORD IDord-ce729fb729ad438ca1ac2e3c7d45e9a4
Source noteuspto-grants-1976_07