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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972711Generated: November 3, 2026

Benzylamine → HCID 58529366, compound

https://huagongshe.com/reaction/1972711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantSodium HydroxideHCID 14798—
ReactantTriethyl phosphiteHCID 31215—
Reactant1-(4-Chloro-2-nitrophenyl)ethan-1-oneHCID 12643796—
CatalystTitanium isopropoxideHCID 11026—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 58529366HCID 5852936662%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 1-(4-chloro-2-nitrophenyl)ethanone (12.5 g, 63 mmol) and benzylamine (13.7 g, 125 mmol) in 200 mL toluene was treated with titanium(IV) isopropoxide (53.5 g, 188 mmol) and heated at 60° C. for 16 h. The solvent was removed in vacuo and the residue taken up in triethylphosphite (31 g, 187 mmol) and the mixture heated cautiously to 150° C. for 2 h. The reaction was cooled to rt and diluted with 30 mL absolute ethanol. 3 mL of 4N aq NaOH was added dropwise with vigorous stirring. After 5 min, the solids were filtered off and the solution diluted with 60 mL absolute ethanol and 60 mL 1N aq NaOH. After stirring overnight, the ethanol was removed in vacuo and the residue diluted with water. Filtration gave the desired product as a dark brown solid (9.86 g, 62%) 1H-NMR (DMSO): δ 7.72 (dd, 1H, J=9, 1 Hz), 7.61 (dd, 1H, J=2, 1 Hz), 7.23 to 7.36 (m, 3H), 7.15 to 7.20 (m, 2H), 6.96 (dd, 1H, J=9, 2 Hz), 5.60 (s, 2H), 2.58 (s, 1H); MS: LC/MS (+esi): m/z=275.1 [MH]+; LC/MS rt=3.51 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-e95b1e9a37d64f2ba7c42c031ef9e688
Source noteuspto-grants-2013_04