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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489542Generated: October 31, 2026

Pyridine → 2-Bromoethyl octanoate

https://huagongshe.com/reaction/1489542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOctanoyl chlorideHCID 8124—
Reactant2-BromoethanolHCID 10898—
SolventBenzeneHCID 241—
Product2-Bromoethyl octanoateHCID 22988381%

Reaction Steps

2-Bromoethanol (4 g, 32 mmol) was added dropwise to a solution of octanoyl chloride (7.8 g, 48 mmol) and pyridine (5 mL) in benzene (50 mL). The reaction mixture was stirred at room temperature for 24 hours. After evaporation of benzene and pyridine under high vacuum, the residue was redissolved in benzene (100 mL). The solution was washed with water (50 mL), sulfuric acid solution (3×25 mL, 0.5N), sodium bicarbonate solution (25 mL, 1N), and water (2×75 mL). The benzene layer was dried over Na2SO4. The drying agent was suction filtered, and the benzene was evaporated. The resulting oil was purified by silica gel chromatography using chloroform/methanol (9:1) to give 6.5 g of pure product. Yield 81%; liquid; IR (neat) 2930 and 2850 (aliphatic CH), 1730 (CO ester) cm-1 ; 1H NMR (CDCl3) 0.85-0.95 (t, CH3 (CH2)4), 1.20-1.40 (m, CH3 (CH2)4), 1.55-1.70 (m, CH2 CH2 CO), 2.25-2.40 (t, CH2 CH2 CO), 3.50-3.60 (t, O CH2 CH2 Br), 4.35-4.40 (t, O CH2 CH2 Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05679684
Source datasetuspto-grants-1997_10
ORD IDord-f059476046b2459ea37b4e42da564690
Source noteuspto-grants-1997_10