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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Boc-D-Asp(OBzl)-OH | HCID 6994663 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-3-tert-butoxycarbonylamino-N,N-dimethyl-succinamic acid benzyl ester | HCID 68990953 | 71.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344027B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-bb98adc28fca492392c4eecb0cdd9cb0 |
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| Source note | uspto-grants-2013_01 |
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