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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445068Generated: November 2, 2026

Benzyl Bromide → HCID 67141681, compound

https://huagongshe.com/reaction/1445068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant18-Crown-6HCID 28557—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67141977HCID 67141977—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67141681HCID 6714168170.9%

Reaction Steps

18-Crown-6 (2 mg, 0.006 mmol) and potassium tert-butoxide (7 mg, 0.066 mmol) were added to a solution of 7-(4-chlorophenyl)-3-ethoxymethyl-2-methyl-1H-pyrrolo[2,3-c]pyridine (20 mg, 0.066 mmol) prepared in Example 466 in anhydrous tetrahydrofuran (1 ml). The reaction mixture was stirred for 30 minutes at room temperature and then benzyl bromide (11.8 μl, 0.099 mmol) was added thereto. The reaction mixture was stirred overnight and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (ethyl acetate/n-hexane=1/5, v/v). The resulting product was dissolved in ethyl acetate, saturated with hydrochloric acid gas, and then filtered to give 10 mg of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662832B2
Source datasetuspto-grants-2010_02
ORD IDord-cc6e2505dd0d406bb1534aa43b18d33c
Source noteuspto-grants-2010_02