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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392033Generated: November 1, 2026

Ethyl orthoformate → Allyl 3-(methylamino)benzoate

https://huagongshe.com/reaction/1392033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantAllyl 3-aminobenzoateHCID 18930599—
CatalystTrifluoroacetic acidHCID 6422—
ProductAllyl 3-(methylamino)benzoateHCID 2216860917%

Reaction Steps

Allyl 3-aminobenzoate (5 g, 28.2 mM) was dissolved in triethyl orthoformate (50 ml) and trifluoroacetic acid (5 drops) was added. The soluiton was stirred and refluxed up through 3a molecular sieves for 5 hours. Solvent was removed, and the residue dissolved in ethanol (50 ml), followed by the addition of acetic acid (8.08 ml) and sodium cyanoborohydride (6.85 g, 0.108 M) in several portions. The mixture was stirred at ambient temperature for 16 hours, and solvent removed. The residue was dissolved in diethyl ether, washed with water, brine, and dried over MgSO4. Crude product was purified by chromatography on silica, eluting with a gradient from dichloromethane to dichloromethane/ethyl acetate (95:5), to give allyl 3-methylaminobenzoate (0.93 g, 17%). Nmr (CDCl3): δ 2.88 (s, 3H); 4.81 (dt, 2H); 5.23-5.45 (m, 2H); 5.94-6.13 (m, 1H); 6.83 (dd, 1H); 7.25 (dd, 1H); 7.33 (t, 1H); 7.43 (dm, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342005B2
Source datasetuspto-grants-2008_03
ORD IDord-a3ae3000d8604798aa8a67b3b4760d9c
Source noteuspto-grants-2008_03