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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361029Generated: October 30, 2026

Hydrochloric Acid → HCID 57489778, compound

https://huagongshe.com/reaction/1361029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantm,alpha-DichlorotolueneHCID 12103—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57457071HCID 57457071—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57489778HCID 57489778—

Reaction Steps

3-[2-(Triphenylmethyl)-2H-tetrazol-5-yl]-9H-carbazole (200 mg, 0.42 mmol) was dissolved in methyl sulfoxide (1.5 mL). Sodium hydride (34 mg, 60%, 0.85 mmol) was added, and the resulting suspension was stirred for 30 min at room temperature. 3-Chlorobenzyl chloride (85 μL, 108 mg, 0.67 mmol) was added, and the stirring was continued at 40° C. for 18 hours. The reaction mixture was cooled to ambient temperature and poured into 0.1 N hydrochloric acid (aq.) (15 mL) The precipitated solid was filtered off and washed with water (3×10 mL) to furnish 9-(3-chlorobenzyl)-3-[2-(triphenylmethyl)-2H-tetrazol-5-yl]-9H-carbazole, which was dissolved in a mixture of tetrahydrofuran and 6 N hydrochloric acid (aq.) (9:1) (10 mL) and stirred at room temperature for 18 hours. The reaction mixture was poured into water (100 mL). The solid was filtered off and rinsed with water (3×10 mL) and dichloromethane (3×10 mL) to yield the title compound (127 mg). No further purification was necessary.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879893B2
Source datasetuspto-grants-2011_02
ORD IDord-77b33dde587f4ba78e436de960aa0730
Source noteuspto-grants-2011_02