Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732040Generated: October 30, 2026

Benzoyl chloride, 3-chloro- → 1-[5-(3-Chlorophenyl)-1,2,4-oxadiazol-3-yl]ethanol

https://huagongshe.com/reaction/732040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
ReactantN',2-dihydroxypropanimidamideHCID 5063567—
SolventPyridineHCID 1049—
Product1-[5-(3-Chlorophenyl)-1,2,4-oxadiazol-3-yl]ethanolHCID 5783794160%

Reaction Steps

To a solution of 3.19 g (30.6 mmol) 2,N-dihydroxy-propionamidine in 25 ml pyridine was added 4.3 ml (33.7 mmol) 3-chloro-benzoyl chloride at 0° C. Cooling was removed and the mixture was stirred at room temperature for 25 min and at reflux for 25 min. After cooling the mixture was poured into water and extracted twice with CH2Cl2. The organic phase was dried and concentrated. Recrystallization from heptane/EtOAc afforded 4.12 g (60%) of a white solid. 1H NMR (CDCl3), d (ppm): 1.68 (d, 3 H) 2.67 (m, 1 H) 5.09 (m, 1 H) 7.46 (t, 1 H) 7.56 (d, 1 H) 8.01 (d, 1 H) 8.13 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585881B2
Source datasetuspto-grants-2009_09
ORD IDord-b258066a0f9a4328b039ba4f779c16d4
Source noteuspto-grants-2009_09