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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816487Generated: October 30, 2026

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

https://huagongshe.com/reaction/1816487

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 numberUS06884796B2
Source datasetuspto-grants-2005_04
ORD IDord-bd95cea129e747cf89c431582940f4d1
Source noteuspto-grants-2005_04