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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918418Generated: November 2, 2026

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

https://huagongshe.com/reaction/918418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthane, 2-diazo-1,1-diethoxy-HCID 21520892—
Reactant11beta,16alpha,17,21-Tetrahydroxy-6alpha-methylpregna-1,4-diene-3,20-dioneHCID 68129099—
Product16alpha-[(2,2-Diethoxy)ethoxy]-11beta,17,21-trihydroxy-6alpha-methylpregna-1,4-diene-3,20-dioneHCID 22791780—

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 11β,16α,17,21-tetrahydroxy-6α-methylpregna-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-7f21642a8a214e3e94911cc69ec1c3ab
Source noteuspto-grants-1976_07