Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457037Generated: November 2, 2026

Tributylstannane → HCID 22103417, compound

https://huagongshe.com/reaction/1457037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHCID 54310283HCID 54310283—
ReactantHCID 86753405HCID 86753405—
SolventTolueneHCID 1140—
ProductHCID 22103417HCID 2210341723.6%

Reaction Conditions

Temperature75 °C

Reaction Steps

5-Methyl-1-[3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]3-propyl]-1,2,4-triazole (I, Azo=5-methyl-1,2,4-triazol-1-yl, Y=1,3-propylene, R1,R2 =3,5-dimethyl, R3 =2-methyl-tetrazol-5-yl) p To a solution of 5-phenoxythiocarbonyloxymethyl-1-[3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propyl]-1,2,4-triazole (130 mg, 0.79 mmol) in 20 ml of toluene was added AIBN (130 mg, 0.79 mmol) and tributyltin hydride (3.2 g, 11 mmol) and the mixture was stirred at 75° C. for 6.5 h. The solvent was concentrated in vacuo and the residue was purified by silica column chromatography (13 cm column, ethyl acetate/hexane, 1/1-5/1; methylene chloride/acetone, 4/1-0/1) to afford 61 mg (19%) of 5-methyl-1-[3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propyl]-1,2,4-triazole, m.p. 126°-128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846986
Source datasetuspto-grants-1998_12
ORD IDord-d1ae866b964145fe962eefec752b3639
Source noteuspto-grants-1998_12