Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230388Generated: October 30, 2026

Benzyl Chloride → HCID 10161821, compound

https://huagongshe.com/reaction/230388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantTriethylamineHCID 8471—
ReactantHCID 67214147HCID 67214147—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 10161821HCID 101618215%

Reaction Conditions

Temperature23 °C

Reaction Steps

Triethylamine (0.83 ml; 0.006 mol) was added at about 23° C. to a solution of (1R)-1-(1-benzyl-4-tert-butyl-1H-imidazol-2-yl)-2-(1H-indol-3-yl)ethanamine (0.7 g; 0.002 mol; prepared according to experimental conditions analogous to the preceding examples and using the appropriate starting compounds and reaction products) in 15 ml acetonitrile. The mixture was agitated about one hour at about 23° C. and benzyl chloride (0.23 ml; 0.002 mol) was added. Agitation was maintained for about 16 hours. The reaction mixture was concentrated using a rotative evaporator and the oil obtained was taken up in ethyl acetate and water. The aqueous phase was extracted with ethyl acetate and washed with water and then with a saturated solution of sodium chloride. The solvents were evaporated under vacuum. After purification over a silica column (eluent: ethyl acetate-heptane/7-3), a strong beige solid was obtained in the form of a glue (yield of 5%). Free base. Melting point: 60-62° C. MH+=463.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566734B2
Source datasetuspto-grants-2009_07
ORD IDord-5552549c3a7244c2a7f25a78047820a8
Source noteuspto-grants-2009_07