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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzoxazole | HCID 11986 | — |
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Tert-butyl 2-(benzo[d]oxazol-2-ylamino)ethylcarbamate | HCID 47453718 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481547B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-6c940d0472ba490c9940a6b75fb13a00 |
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| Source note | uspto-grants-2013_07 |
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