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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625976Generated: October 26, 2026

Hydrochloric Acid → HCID 136199556, compound

https://huagongshe.com/reaction/625976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant2-MercaptobenzonitrileHCID 11018926—
SolventDimethylformamideHCID 6228—
ProductHCID 136199556HCID 13619955646%

Reaction Steps

In a 250 mL round bottom flask was added 2-mercaptobenzonitrile (2.0 g, 14.8 mmol) from Step 1(B) followed by anhydrous DMF (30 mL). Ammonium chloride (1.42 g, 26.64 mmol) and sodium azide (1.73 g, 26.64 mmol) were added to the reaction flask followed by an additional 10 mL of DMF. The reaction mixture was heated to 105° C. under a flow of N2 and stirred overnight. The reaction was worked up by first cooling to room temperature. Next the solution was acidified by the addition of 50 mL of 1N HCl. The solution was extracted with ethyl acetate (2×100 mL) and then washed with brine (100 mL). The combined organics were dried over Na2SO4 and then concentrated under reduced pressure to afford a white solid. The solid was collected by filtration of a heptane/ethyl acetate treatment (7:3, 10 mL) which afforded the title compound as a white solid (1.21 g, 46%); Rf of 0.05″ with 95:5 v/v dichloromethane: methanol; 1H-NMR (400 MHz; DMSO-d6) δ 7.91 (d, 1H), 7.78 (d, 1H), 7.64-7.50 (m, 2H), 2.90 (s, 1H), 2.78 (s, 1H); MS (ESI−) m/z 177.1 (Mz−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309203B2
Source datasetuspto-grants-2016_04
ORD IDord-51893c719d544d23aba514c5d8c1dea4
Source noteuspto-grants-2016_04