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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512231Generated: November 4, 2026

2-Methylbenzylamine → HCID 11652890, compound

https://huagongshe.com/reaction/1512231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylbenzylamineHCID 6993—
ReactantSodium AzideHCID 33557—
Reactant2,3-Dichlorophenyl IsothiocyanateHCID 2796281—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11652890HCID 11652890—

Reaction Steps

2-Methylbenzylamine (89.1 mg, 0.735 mmol) in 8 ml of dry THF was treated with 2,3-dichlorophenylisothiocyanate (150 mg, 0.735 mmol). After stirring at room temperature for 1 hour, the mixture was treated with mercuric acetate (234.2 mg, 0.735 mmol) and sodium azide (143.3 mg, 2.21 mmol) and stirred at room temperature for 16 hours. The mixture was filtered through a pad of Celite and washed with ethyl acetate. The filtrate was concentrated under reduced pressure and purified by preparative HPLC on a Waters Symmetry C8 column (40 mm×100 mm, 7 μm particle size) using a gradient of 10% to 100% acetonitrile to ammonium acetate (10 mM) over 15 minutes at a flow rate of 70 mL/min to provide the title compound. MS (ESI+) m/z 334 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 2.29 (s, 3H), 4.46 (d, J=5.42 Hz, 2H), 7.16 (m, 3H), 7.26 (m, 1H), 7.57 (t, J=5.42 Hz, 1H), 7.60 (t, J=8.14 Hz, 1H), 7.71 (dd, J=7.97, 1.53 Hz, 1H), 7.93 (dd, J=8.14, 1.70 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217067B2
Source datasetuspto-grants-2012_07
ORD IDord-8c10142f4b7941dab4abdeec300a9a95
Source noteuspto-grants-2012_07