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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886932Generated: October 31, 2026

Triethylamine → 2-(4-Chlorobenzylthio)-5-nitrobenzo[d]oxazole

https://huagongshe.com/reaction/1886932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
Reactant5-Nitrobenzo[D]Oxazole-2-ThiolHCID 786293—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
Product2-(4-Chlorobenzylthio)-5-nitrobenzo[d]oxazoleHCID 6733258478%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 5-nitrobenzo[d]oxazole-2(3H)-thione (196.2 mg, 1.0 mmol) in chloroform (10 mL) was added triethylamine (278 μL, 2 mmol) followed by 1-(bromomethyl)-4-chlorobenzene (226 mg, 1.1 mmol). The reaction was stirred at 60° C. for 2 h. After cooling, the reaction was diluted with ethyl acetate, washed with dilute aqueous hydrochloric solution and brine. The combined organic layers were dried over anhydrous MgSO4 and evaporated. The resulting solid was purified by column chromatography eluting with ethyl acetate/hexanes 1:10 v/v to afford 250 mg (78%) of the title compound (LCMS RT=7.64 min)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501713B2
Source datasetuspto-grants-2013_08
ORD IDord-03cd7ad5b8344986b46bbce4dd5b8b30
Source noteuspto-grants-2013_08