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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260789Generated: November 2, 2026

Ethyl orthoformate → Allyl 3-(methylamino)benzoate

https://huagongshe.com/reaction/2260789

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 3å 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): δ2.88 (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 numberUS05478820
Source datasetuspto-grants-1995_12
ORD IDord-3638f827f95f4cf19339a4675534f619
Source noteuspto-grants-1995_12