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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558306Generated: October 29, 2026

Methylamine → 4-(methylaminomethyl)benzonitrile

https://huagongshe.com/reaction/558306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-(methylaminomethyl)benzonitrileHCID 10606883—

Reaction Steps

4-Cyanobenzaldehyde (12.0 g, 92.0 mmol), methylamine (69 ml of a 2.0M solution in tetrahydrofuran, 137 mmol) and magnesium sulphate (45 g) were stirred in dichloromethane (300 ml) at room temperature for 5 days. The mixture was filtered and the filtrate was concentrated under reduced pressure to leave a yellow oil. The oil was dissolved in methanol (200 ml) and sodium borohydride (4.10 g, 109 mmol) was added cautiously with vigorous stirring. Once the addition was complete the reaction was stirred for 1 hour and the mixture was concentrated under reduced pressure. The residue was dissolved in 1M aqueous sodium hydroxide solution (200 ml) and the mixture was stirred at room temperature for 1 hour. The resulting solution was extracted with dichloromethane (2×200 ml) and the combined organic phases were dried over magnesium sulphate, filtered and concentrated under reduced pressure to provide the title compound (13.4 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063044B2
Source datasetuspto-grants-2011_11
ORD IDord-28708e56b54946a59c94d55c17b55656
Source noteuspto-grants-2011_11