Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867551Generated: November 4, 2026

Ammonia → HCID 57980016, compound

https://huagongshe.com/reaction/1867551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant2,4-OxazolidinedioneHCID 97389—
ReactantHCID 54554517HCID 54554517—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57980016HCID 5798001630.6%

Reaction Steps

A solution of 1.0 g (4 mmol) of [4-(4-phenyl-1H-imidazol-1-yl)phenyl]methanol, prepared in step 12.1., 0.485 g (4.80 mmol) of 1,3-oxazolidine-2,4-dione and 1.15 g (4.38 mmol) of triphenylphosphine in 16 ml of tetrahydrofuran, cooled by a bath of acetone and ice, is admixed dropwise with 0.80 g (4 mmol) of diisopropyl azodicarboxylate in solution in 2 ml of tetrahydrofuran. The mixture is subsequently warmed to ambient temperature again and stirred overnight. 9 ml of the solution are taken, to which are added 12 ml of a 7N ammonia solution (84 mmol) in methanol. The mixture is left to react overnight, admixed with 4 g of silica and evaporated to dryness. The product is purified by chromatography on silica gel, eluting with a 95/5 then 93/7 and 90/10 mixture of dichloromethane and methanol. The product is recrystallized from a mixture of methanol and diisopropyl ether, to give 0.429 g of product in the form of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632850B2
Source datasetuspto-grants-2009_12
ORD IDord-64f9048b327d4659aba5c2f17b8eb530
Source noteuspto-grants-2009_12