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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium HydroxideHCID 14797—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
ReactantMethanedione--ethanol (1/1)HCID 19604758—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product2-[(tert-Butoxy)carbonylamino]-N-(phenylmethoxy)acetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04028401
Source datasetuspto-grants-1977_06
ORD IDord-564b064ae6d147c3b71798fedd0fe5c9
Source noteuspto-grants-1977_06