HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635407Generated: October 30, 2026
Ethyl orthoformate → Allyl 3-(methylamino)benzoate
https://huagongshe.com/reaction/635407
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Allyl 3-aminobenzoate | HCID 18930599 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Product | Allyl 3-(methylamino)benzoate | HCID 22168609 | 17% |
Reaction Steps
Allyl 3-aminobenzoate (5 g, 28.2 mN) was dissolved in triethyl orthoformate (50 ml) and trifluoroacetic acid (5 drops) was added. The solution 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187804B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-4dc3623ad7b84d67bbb53bd8ae54d858 |
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| Source note | uspto-grants-2001_02 |
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