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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1666341Erstellt: 26. Oktober 2026

Pyridine → Phenyl 1H-benzo[d][1,2,3]triazol-5-ylcarbamate

https://huagongshe.com/reaction/1666341

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktPhenyl chloroformateHCID 15891—
EduktHCID 178507366HCID 178507366—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktPhenyl 1H-benzo[d][1,2,3]triazol-5-ylcarbamateHCID 17852183557%

Reaktionsschritte

To a solution of 1H-benzo[d][1,2,3]triazol-5-amine (1.85 g, 13.8 mmol, Alfa Aesar) in THF (10 mL) and CH3CN (8 mL) was added pyridine (1.34 mL, 16.6 mmol) followed by phenyl chloroformate (2.27 mL, 14.5 mmol) slowly. The reaction was stirred overnight. The reaction was concentrated to give an oil, which was partitioned between CH2Cl2 and water. The organic layer was dried using a SPE phase separator and concentrated to give a solid. This was taken up in CH2Cl2 and the precipitate was filtered to give the desired product (2.0 g, 57%) which was used without purification. MS M+1: 256.06.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044052B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-89dbd0b464a34d7d86d04e9bdc9844bb
Quellennotizuspto-grants-2011_10