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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585513Generated: October 29, 2026

Chlorotrimethylsilane → HCID 22866440, compound

https://huagongshe.com/reaction/1585513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant3-Hydroxyspirostan-11-oneHCID 73682—
Reactant2-Amino-3,4-dimethylpyridineHCID 11007884—
SolventDichloromethaneHCID 6344—
ProductHCID 22866440HCID 2286644085%

Reaction Steps

Trimethylsilylchloride (3.27 mL, 25.8 mmol) was added to a solution of (3β,5α,25R)3-hydroxy-spirostan-11-one (4.0 g, 9.3 mmol) and triethylamine (6.5 mL, 46 mmol) in dichloromethane (60 mL) at room temperature. One gram of dimethyl aminopyridine was added and the reaction was stirred at room temperature for 12 hours. The reaction was quenched with methanol (1 mL) and diluted with ethyl acetate, washed with water (5×) and brine (1×), dried (Na2SO4), filtered and concentrated in vacuo. The product was triturated with methanol, filtered and dried to afford 3.94 g (85%) product as a white solid. 1H NMR (250 MHz, CDCl3) 6 4.5 (q, 1H, J=6Hz); 3.45 (m, 2H); 2.35 (t, 1H, J=10 Hz); 2.4 (dt, 1H, J=12.2 Hz); 2.2 (s, 2H); 2.1-1.1 (m, 12H); 1.02 (s, 3H); 0.9 (d, 3H, J=7.0 Hz); 0.78 (d, 3H, J=7 Hz); 0.69 (s, 3H); 0.1 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939398
Source datasetuspto-grants-1999_08
ORD IDord-36bb5a9dca834f679f393e0bba651ff9
Source noteuspto-grants-1999_08