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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132707Generated: October 25, 2026

Pyridine → 1,2-butandiol Dibenzoate

https://huagongshe.com/reaction/132707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantTetrahydrofuranHCID 8028—
Reactant1,2-ButanediolHCID 11429—
SolventWaterHCID 962—
Product1,2-butandiol DibenzoateHCID 23125906—

Reaction Steps

To the reactor were added 1,2-butylene-glycol (2.5 g), benzoyl chloride (7.8 g), pyridine (8.8 g) and tetrahydrofuran (70 ml). The reactants was mixed and heated refluxing for 4 hours, then cooled to room temperature. Water was added to the reaction system until the inorganic phase was transparent. Organic phase was separated. Inorganic phase was extracted with ethyl ether. The combined organic phase was washed with water, dried over anhydrous sodium sulfate. After concentrated, 3.95 g product was separated. 1H-NMR: δ (ppm)1.0-1.1 (3H), 1.7-1.9(2H), 4.4-4.6(2H), 5.4-5.5(1H) and 7.4-8.2(10H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388061B2
Source datasetuspto-grants-2008_06
ORD IDord-b78bc78a8a854a8a814d4a63cfdec3ef
Source noteuspto-grants-2008_06