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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707960Generated: October 25, 2026

Benzyl Alcohol → HCID 11735856, compound

https://huagongshe.com/reaction/1707960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPyridineHCID 1049—
Reactant2-Methyl-4-pentenoyl chlorideHCID 12921442—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 11735856HCID 1173585678.3%

Reaction Steps

To a 0° C. solution of 23.8 g of benzyl alcohol, 0.05 g of 4-(dimethylamino)pyridine, 18.3 g of pyridine and 250 ml of methylene chloride is added, dropwise, a solution of 29.5 g of racemic 2-methyl-4-pentenoyl chloride in 50 ml of methylene chloride. The mixture is stirred at room temperature for 4 hours, followed by successive washing with 2N hydrochloric acid, saturated sodium bicarbonate and saturated sodium chloride. The organic layer is dried and concentrated in vacuo. The residue is purified by Kugelrohr distillation to give 35.2 g of the desired product as a colorless oil; bp 70°-75° C. at 0.10 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356885
Source datasetuspto-grants-1994_10
ORD IDord-e034fe3030ad4579aa1c167f3273b062
Source noteuspto-grants-1994_10