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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433668Generated: October 29, 2026

Triethylamine → 2-Tert-butoxycarbonylamino-4-oxo-butyric acid benzyl ester

https://huagongshe.com/reaction/433668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfur trioxide-pyridineHCID 168533—
Reactant2-Tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl esterHCID 11347393—
SolventDimethyl SulfoxideHCID 679—
Product2-Tert-butoxycarbonylamino-4-oxo-butyric acid benzyl esterHCID 14357795—

Reaction Steps

A dimethyl sulfoxide (10 mL) solution of 2-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester (13.58 g, 43.9 mmol) and triethyl amine (18.35 mL, 131.7 mmol) was cooled to 0° C. Pyridine sulfur trioxide (21.0 g. 131.7 mmol) in dimethyl sulfoxide (80 mL) was added in a steady stream. The cooling bath was removed and the reaction stirred 1.5 hours. The reaction was poured into 130 mL ice water and extracted with diethyl ether (2×180 mL and 100 mL). The combined organic portion was washed sequentially with saturated sodium bicarbonate, water, brine and dried over magnesium sulfate. The solvent was removed in vacuo and the crude product was chromatographed on silica gel (900 mL) eluting with ethyl acetate/hexanes (1:4), to give the title compound as a clear, colorless oil (9.20 g, 70%). MS (CI) m/z 208.0 (M−99).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667331B2
Source datasetuspto-grants-2003_12
ORD IDord-1a601c1da20047c792e7808bce94d0ca
Source noteuspto-grants-2003_12