HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436915Generated: October 25, 2026
Triethylamine → 2-[(tert-Butoxy)carbonylamino]-N-(phenylmethoxy)acetamide
https://huagongshe.com/reaction/436915
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | Benzyloxyamine hydrochloride | HCID 102312 | — |
| Reactant | Methanedione--ethanol (1/1) | HCID 19604758 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(tert-Butoxy)carbonylamino]-N-(phenylmethoxy)acetamide | HCID 14694702 | — |
Reaction Steps
O-Benzylhydroxylamine hydrochloride (15.0 g, 93.8 mMol) was dissolved in methanol (150 ml) and added to a solution of potassium hydroxide (5.27 g, 93.8 mMol) in methanol (50 ml). The resulting mixture was cooled, filtered, evaporated, dissolved in tetrahydrofuran (25 ml) and filtered as solution A. t-Butyloxycarbonyl glycine (16.4 g, 93.8 mMol) was dissolved in tetrahydrofuran (75 ml), triethylamine (13.2 ml, 93.8 mMol) added and the solution cooled to -10° C. with dry ice/ethanol. Iso-butyl chloroformate (12.2 ml, 93.8 mMol) was added and the solution stirred cold 2 minutes, before adding solution A dropwise. The mixture was stirred cold 1 hour and at room temperature 2 hours, filtered, evaporated, dissolved in ethyl acetate (100 ml), washed with water (3× 50 ml), dried over magnesium sulfate and evaporated to an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04028401 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-564b064ae6d147c3b71798fedd0fe5c9 |
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| Source note | uspto-grants-1977_06 |
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