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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799599Generated: October 31, 2026

Triethylamine → (R)-3-tert-butoxycarbonylamino-N,N-dimethyl-succinamic acid benzyl ester

https://huagongshe.com/reaction/1799599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantEthyl chloroformateHCID 10928—
ReactantBoc-D-Asp(OBzl)-OHHCID 6994663—
SolventDichloromethaneHCID 6344—
Product(R)-3-tert-butoxycarbonylamino-N,N-dimethyl-succinamic acid benzyl esterHCID 6899095371.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (2.8 mL, 20.0 mmol) was added at 0° C. to a solution of Boc-D-aspartic acid 4-benzyl ester (5.00 g, 15.0 mmol) in dichloromethane, then ethyl chloroformate (1.91 mL, 20.0 mmol) was added dropwise. The reaction mixture was stirred for 1 h at 0° C., then a solution of dimethylamine hydrochloride (2.65 g, 32.0 mmol) and triethylamine (4.53 mL, 32.0 mmol) in dichloromethane (100 mL) were added dropwise. The reaction mixture was allowed to reach room temperature over 16 h, then washed with brine, and concentrated. Chromatography (SiO2; heptane-ethyl acetate gradient) produced (R)-3-tert-butoxycarbonylamino-N,N-dimethyl-succinamic acid benzyl ester (3.77 g, 70%). Colorless oil, m/e=351.4 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344027B2
Source datasetuspto-grants-2013_01
ORD IDord-bb98adc28fca492392c4eecb0cdd9cb0
Source noteuspto-grants-2013_01