HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354495Generated: October 29, 2026
Acetic Acid → methyl 4-[2-(N-benzyloxycarbonyl-N-methylamino)ethylamino]benzoate
https://huagongshe.com/reaction/354495
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl 4-aminobenzoate | HCID 12082 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Benzyl N-methyl-N-(2-oxoethyl)carbamate | HCID 12010768 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | methyl 4-[2-(N-benzyloxycarbonyl-N-methylamino)ethylamino]benzoate | HCID 23511696 | 334.5% |
Reaction Steps
A stirred solution of N-benzyloxycarbonyl-N-methylaminoacetaldehyde (1.77 g, 1.1 mmol) in toluene (3 mL) was added methyl-4-aminobenzoate (1.29 g, 8.5 mmol), and the mixture was stirred for 1 hr at room temp. The reaction mixture was evaporated under a reduced pressure and the residue was dissolved into MeCN (15 mL). To the solution was added AcOH (2.44 mL, 43 mmol) and NaBH3CN (2.67 g, 43 mmol), and the resulting mixture was stirred for 15 hr at room temp. The reaction was quenched by the addition of sat. NaHCO3. The mixture was extracted with EtOAc, washed with brine, dried over MgSO4, and evaporated. The residue was chromatographed on silica-gel with n-hexane: EtOAc (7:3, v/v) as eluent to give 1.26 g (43%) methyl 4-[2-(N-benzyloxy carbonyl-N-methylamino)ethylamino]benzoate as a colorless oil. 1H-NMR (CDCl3, 400 MHz) δ2.96 (s, 3H), 3.32 (br m, 2H), 3.50-3.60 (m, 2H), 3.82 (s, 3H), 5.15 (each d, 2H, J=14.6 Hz), 6.35 and 6.58 (m, total 2H), 7.36 (s, 5H), 7.76 and 7.84 (m, total 2H); MS (FAB) m/z 342 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06756378B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-de2aa24645be4fc6b8cef0088cb51523 |
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| Source note | uspto-grants-2004_06 |
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