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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386670Generated: October 31, 2026

Acetonitrile → HCID 178465564, compound

https://huagongshe.com/reaction/386670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantHCID 58097574HCID 58097574—
ProductHCID 178465564HCID 17846556473%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-[(4-(imidazol-1-yl)-phenyl]-3-benzyloxy-6-amino-4H-1-benzopyran-4-one (3 g; 6.22 mmol) was suspended in acetonitrile (50 mL) and cooled at 0° C. HCl was bubbled into the solution upon saturation. The reaction was then stirred for 4 hours at r.t., upon completion, H2O (20 mL) was added and the acetonitrile removed under vacuum. The solution was then brought to pH=9 with NaOH 2N, the precipitate was filtered off and dried to give the titled compound as a bright yellow solid. Yield: 73%. TLC: (9/1 Chloroform/Methanol) Rf: 0.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372866B2
Source datasetuspto-grants-2013_02
ORD IDord-1441483351074a40bdf9209f95e30903
Source noteuspto-grants-2013_02