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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187274Generated: October 30, 2026

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

https://huagongshe.com/reaction/2187274

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 numberUS06407086B2
Source datasetuspto-grants-2002_06
ORD IDord-86269ca5c79f4ba2babce669fefe7df9
Source noteuspto-grants-2002_06