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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl 4-aminobenzoateHCID 12082—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantBenzyl N-methyl-N-(2-oxoethyl)carbamateHCID 12010768—
SolventTolueneHCID 1140—
Productmethyl 4-[2-(N-benzyloxycarbonyl-N-methylamino)ethylamino]benzoateHCID 23511696334.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756378B2
Source datasetuspto-grants-2004_06
ORD IDord-de2aa24645be4fc6b8cef0088cb51523
Source noteuspto-grants-2004_06