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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694375Generated: October 26, 2026

Boron trifluoride etherate → Methyl 4-(1-aminocyclopropyl)benzoate

https://huagongshe.com/reaction/1694375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantMethyl 4-cyanobenzoateHCID 70791—
ReactantHCID 178461630HCID 178461630—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-(1-aminocyclopropyl)benzoateHCID 4514020943%

Reaction Steps

Methyl 4-cyanobenzoate (2.6 kg, 16.1 mol) was dissolved in 40 L of toluene at −25° C. and Ti(Oi-Pr)4 (4.73 L, 16.1 mol) was added over 5 min, followed by EtMgBr (10.5 L of a 3.07M solution in THF, 32.3 mol) over 2 hr. After aging for 30 min, BF3.OEt2 (4.1 L, 32 mol) was added over 40 min and the mixture was aged for another 40 min. The reaction was quenched by the addition of 40 L of 3N HCl. The layers were separated and the aqueous layer was washed with 13 L toluene. The aqueous layer was then extracted with 2-MeTHF (2×26 L and 2×13 L). The combined 2-MeTHF layers were washed with 3N NaOH and the pH of the NaOH layer adjusted to 9 before separation of the layers. The organic layer was washed with 13 L of brine. Yield=43%. 1H NMR (500 MHz, CDCl3): δ 8.00 (d, 2H), 7.35 (d, 2H), 3.95 (s, 3H), 1.25 (t, 2H), 1.10 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158671B2
Source datasetuspto-grants-2012_04
ORD IDord-2b4be886d5c54c15811377e8cb9bff9f
Source noteuspto-grants-2012_04