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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447144Generated: October 30, 2026

2-Chlorobenzoxazole → Tert-butyl 2-(benzo[d]oxazol-2-ylamino)ethylcarbamate

https://huagongshe.com/reaction/447144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
ReactantN-BOC-ethylenediamineHCID 187201—
SolventChloroformHCID 6212—
ProductTert-butyl 2-(benzo[d]oxazol-2-ylamino)ethylcarbamateHCID 47453718—

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 2-chlorobenzoxazole (0.6 mL, 5.16 mmol) and N-(2-aminoethyl) carbamic acid tert-butyl ester (2.4328 g, 15.18 mmol)) was stirred in a preheated oil bath at 125° C. for 5 h, then held at room temperature overnight. The solidified mixture was dissolved in chloroform (125 mL), washed with aqueous sodium bicarbonate (2×150 mL), then brine (1×150). The organic layer was dried over sodium sulfate, then filtered and concentrated in vacuo. The resulting residue was purified by flash column chromatography, eluting with 60% ethyl acetate in heptane to yield tert-butyl 2-(benzo[d]oxazol-2-ylamino)ethylcarbamate as a beige powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481547B2
Source datasetuspto-grants-2013_07
ORD IDord-6c940d0472ba490c9940a6b75fb13a00
Source noteuspto-grants-2013_07