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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764956Generated: November 2, 2026

1,3-Dibromo-5,5-dimethylhydantoin → 3beta,24-Bis(tert-butyldimethylsilyloxy)-4,4-dimethylchola-5,7-diene

https://huagongshe.com/reaction/1764956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5,5-dimethylhydantoinHCID 6479—
Reactant3beta,24-Bis(tert-butyldimethylsilyloxy)4,4-dimethylchol-5-eneHCID 15543090—
SolventBenzeneHCID 241—
SolventHexaneHCID 8058—
Product3beta,24-Bis(tert-butyldimethylsilyloxy)-4,4-dimethylchola-5,7-dieneHCID 6941299888.9%

Reaction Steps

3β,24-Bis(tert-butyldimethylsilyloxy)-4,4-dimethylchol-5-ene (44 g) is dissolved in a warm mixture of hexane (2 l) and benzene (540 ml). 1,3-Dibromo-5,5-dimethylhydantoin (15.32 g) is added and the mixture is refluxed for 20 min and then cooled rapidly to room temperature, and the insoluble material is removed by filtration. The filtrate is concentrated under reduced pressure and o-xylene (2 l) and quinaldine (84 ml) is added. The mixture is refluxed for 1 hour. After aqueous work-up and trituration with methanol, 3β,24-bis (tert-butyldimethylsilyloxy)-4,4-dimethylchola-5,7-diene (39 g) is isolated. Melting point: 98-106° C. 1H-NMR (CDCl3, 400 MHz): δ=5.9 (1H, m); 5.54 (1H, m); 3.58 (2H, m); 3.35 (1H, m); 0.91 (18H, s); 0.05 (12H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039678E1
Source datasetuspto-grants-2007_06
ORD IDord-576a977ce06f4ae98d24808f644a1451
Source noteuspto-grants-2007_06