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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024667Generated: October 28, 2026

Benzyl Alcohol → HCID 131731397, compound

https://huagongshe.com/reaction/1024667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant5-Bromovaleric acidHCID 16368—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 131731397HCID 131731397—

Reaction Steps

A solution of 5-bromopentanoic acid (1.00 g, 5.52 mmol) and benzyl alcohol (0.286 mL, 2.76 mmol) in methylene chloride (14 mL) was treated sequentially with N,N′-diisopropylcarbodiimide (0.523 g, 4.14 mmol) and 4-dimethylaminopyridine (43.9 mg, 0.359 mmol). The solution was allowed to stir at room temperature. A precipitate formed within 1 minute of the addition of the 4-dimethylaminopyridine. After ˜65 h, the reaction mixture was filtered, the solid was washed with CH2Cl2 and the filtrate was washed with 20 mL portions of 1N HCl, sat NaHCO3 and brine and dried over Na2SO4. The solution was filtered and concentrated to yield a nearly colorless liquid along with a solid (DIC urea). The material was taken up in 1/1 MTBE/heptane to yield a solution with a white precipitate. The mixture was filtered and concentrated and the crude material was purified by flash chromatography (75 g silica gel; 5-10% MTBE/hept) to yield the title compound (0.69 g, 92%) as a colorless liquid. HPLC purity>95° A) (ret. time, 4.73 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722877B2
Source datasetuspto-grants-2014_05
ORD IDord-48d3b3d75a1f47ca8303c283801ef421
Source noteuspto-grants-2014_05