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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358252Generated: November 1, 2026

Benzyl Alcohol → HCID 11152485, compound

https://huagongshe.com/reaction/2358252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantNitrogenHCID 947—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 58911253HCID 58911253—
SolventTolueneHCID 1140—
ProductHCID 11152485HCID 11152485—

Reaction Conditions

Temperature90 °C

Reaction Steps

In a three necked flask, under argon, a solution of 1-[(2-oxo-4-propylpyrrolidin-1-yl)methyl]-1H-imidazole-5-carboxylic acid a32 (0.35 g, 1.39 mmol, predried by azeotropic distillation with toluene), diphenylphosphoryl azide (0.58 g, 2.1 mmol) and Et3N (0.29 ml) in toluene (5 ml) is heated at 40° C. with formation of N2. The temperature is kept at 40° C. for 4 h and benzyl alcohol (0.301 g, 0.21 mmol) is added. The solution is heated at 90° C. for 1 h, cooled down to room temperature, stirred 48 h, heated at 90° C. for 1 h and concentrated in vacuo. The crude carbamate is purified by chromatography on silicagel (CH2Cl2/MeOH) to afford benzyl 1-[(2-oxo-4-propylpyrrolidin-1-yl)methyl]-1H-imidazol-5-ylcarbamate 83 (0.011 g) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763644B2
Source datasetuspto-grants-2010_07
ORD IDord-4d90b981fa8c4c8883aaa286b7b5d382
Source noteuspto-grants-2010_07