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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215186Generated: October 25, 2026

2-Chlorobenzoxazole → N-(Benzoxazol-2-yl)-N-3-(4-methoxyphenoxy)propyl-3-tert-butyldimethylsilyloxybenzylamine

https://huagongshe.com/reaction/2215186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
ReactantDiisopropylethylamineHCID 81531—
Reactantn-3-(4-Methoxyphenoxy)propyl-3-tert-butyldimethylsilyloxybenzylamineHCID 21949684—
SolventDimethylformamideHCID 6228—
ProductN-(Benzoxazol-2-yl)-N-3-(4-methoxyphenoxy)propyl-3-tert-butyldimethylsilyloxybenzylamineHCID 21949679—

Reaction Steps

N-3-(4-methoxyphenoxy)propyl-3-tert-butyldimethylsilyloxybenzylamine (1.9 g, 5.0 mmol) was dissolved in N,N-dimethylformamide (3.0 mL). Subsequently, N,N-diisopropylethylamine (768 mg, 5.9 mmol) was added dropwise thereto. To the solution, 2-chlorobenzoxazole (912 mg, 5.94 mmol) was added. The mixture was stirred for 15 minutes at room temperature, and then stirred overnight at 70° C. The resultant mixture was extracted with ethyl acetate, followed by washing the organic layer with brine, drying over anhydrous sodium sulfate, and concentration under reduced pressure. The resultant mixture was subjected to purification by silica gel column chromatography (n-hexane/ethyl acetate=10/1), whereby the target compound was obtained (1.9 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109226B2
Source datasetuspto-grants-2006_09
ORD IDord-0925f329851543c29b0a66809d97d3d7
Source noteuspto-grants-2006_09