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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650761Generated: October 30, 2026

Sodium Azide → HCID 178488384, compound

https://huagongshe.com/reaction/650761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 16708548HCID 16708548—
ReactantHCID 18703878HCID 18703878—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178488384HCID 17848838456%

Reaction Steps

To THF (2.5 ml) at −78° C. under an argon atmosphere was added aluminum chloride (90 mg, 0.67 mmol). After slowly warming to room temperature, sodium azide (130 mg, 2.2 mmol) was added, and the resulting mixture was heated at 70° C. for 5 min, then cooled to room temperature. To the reaction mixture was added a solution of (1RS, 2SR, 3SR)-1-(4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carbonitrile (125 mg, 0.34 mmol) in THF (2.5 ml). After heating at 70° C. overnight, thin layer chromatographic analysis of the reaction mixture indicated the presence of starting material, so additional Al(N3)3 was prepared as above (1.34 mmol) in THF. To this was added the reaction mixture, and heating at 70° C. was resumed for an additional 5 h. The mixture was partitioned between EtOAc and 3M HCl. The aqueous phase was extracted with EtOAc, and the combined organic extracts were washed successively with H2O and saturated aqueous NaCl and dried. The solvent was removed in vacuo, and the residue was crystallized from EtOAc/hexanes to afford the title compound (78 mg, 56%). A portion of this material was further purified by MPLC (LiChroprep RP-18, MeOH/H2O=60/40) and then recrystallized; m.p. 155-157° C. (EtOAc/hexanes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274737B1
Source datasetuspto-grants-2001_08
ORD IDord-b04d3ff99934429da1404b6a1b1462f8
Source noteuspto-grants-2001_08