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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855238Generated: October 26, 2026

Water → N'-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamine

https://huagongshe.com/reaction/855238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-tert-ButylbenzaldehydeHCID 70324—
Reactant1,2-Ethanediamine, N1-ethyl-N1-(3-methylphenyl)-HCID 87984—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductN'-(4-tert-butyl-benzyl)-N-ethyl-N-m-tolyl-ethane-1,2-diamineHCID 6934286595%

Reaction Steps

1.62 g (10 mmol) of 4-tert-butyl benzaldehyde and 1.78 g (10 mmol) of N*1*-ethyl-N*1* -m-tolyl-ethane-1,2-diamine were dissolved in 20 ml methanol and the solution was stirred for 2 h at rt. 567 mg (15 mmol) of sodium borohydride were added in portions under nitrogen. The reaction mixture was stirred at rt over night. Water was added and the solvent was evaporated. The reaction mixture was extracted with diethyl ether and the organic layer was washed with saturated aqueous NaCl solution, dried over sodium sulfate, filtered and the solvent was evaporated to leave the 3.08 g (95%) product as a light yellow oil. 1H NMR (DMSO-d6, 300 MHz): δ 7.33 (d, 2H), 7.24 (d, 2H), 7.09 (dd, 1H), 6.51 (m, 3H), 3.78 (s, 2H), 3.42 (t, 2H), 3.34 (q, 2H), 2.85 (t, 2H), 2.29 (s, 3H), 1.31 (s, 9H), 1.11 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-f8163ec0f6c446e3a9d9efb6fbe68099
Source noteuspto-grants-2007_08